510(k) · Cleared
ClearedPRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Primed Medical Products, Inc. · FRG Wrap, Sterilization
Cleared on May 24, 2024 as substantially equivalent to K181174 (Cardinal Health200, LLC, 2018) after a 182-day review. Its family tree reaches back 10 generations to 1988. 1 later device descends from it.
- Decided
- May 24, 2024
- Review
- 182 days
- Class
- Class II
- Product code
- FRG
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 10 generations to K881471 (1988). 17 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 10 generations backK881471 Kimguard (Regular & Heavy Duty) Sterile WrapKimberly-Clark Corp. · 1988 · Recalled
- 6 generations between
- 3 generations backK132060 Durablue Sterilization WrapCardinal Health-Medical Products and Services · 2013
- 2 generations backK151788 Cardinal Health Sterilization WrapCardinal Health200, LLC · 2015
- 1 generation backK181174 Cardinal Health Sterilization WrapCardinal Health200, LLC · 2018
- This deviceK233777 PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600)Primed Medical Products, Inc. · 2024
- Descendant · cites it directly · 0 of its ownK242208 PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600)Primed Medical Products, Inc. · 2024
Show all 10 generations
- Root · 10 generations backK881471 Kimguard (Regular & Heavy Duty) Sterile WrapKimberly-Clark Corp. · 1988 · Recalled
- 9 generations backK082177 Kimguard One-Step Sterilization WrapKimberly-Clark Corp. · 2009
- 8 generations backK091685 Kimguard One-Step Sterilization Wrap, Models KC100, KC200, KC300…Kimberly-Clark Corp. · 2009
- 7 generations backK112211 Dura Blue Sterilization WrapCardinal Health200, LLC · 2011
- 6 generations backK120658 Durablue Sterilization WrapCardinal Health200, LLC · 2012
- 5 generations backK122507 Durablue Sterilization Wrap, Model Numbers CH100, CH200, CH300…Cardinal Health200, LLC · 2012
- 4 generations backK123857 Durablue Sterilization WrapCardinal Health200, LLC · 2013
- 3 generations backK132060 Durablue Sterilization WrapCardinal Health-Medical Products and Services · 2013
- 2 generations backK151788 Cardinal Health Sterilization WrapCardinal Health200, LLC · 2015
- 1 generation backK181174 Cardinal Health Sterilization WrapCardinal Health200, LLC · 2018
- This deviceK233777 PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600)Primed Medical Products, Inc. · 2024
Most influential descendants
Showing 1 of 1 · See all- K242208PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600)Primed Medical Products, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K881471 | Kimguard (Regular & Heavy Duty) Sterile Wrap | Kimberly-Clark Corp. | 1988 | 1 |
| −9 | K082177 | Kimguard One-Step Sterilization Wrap | Kimberly-Clark Corp. | 2009 | — |
| −8 | K091685 | Kimguard One-Step Sterilization Wrap, Models KC100, KC200, KC300, KC400, KC… | Kimberly-Clark Corp. | 2009 | — |
| −7 | K112211 | Dura Blue Sterilization Wrap | Cardinal Health200, LLC | 2011 | — |
| −6 | K120658 | Durablue Sterilization Wrap | Cardinal Health200, LLC | 2012 | — |
| −5 | K122507 | Durablue Sterilization Wrap, Model Numbers CH100, CH200, CH300, CH400, CH500… | Cardinal Health200, LLC | 2012 | — |
| −4 | K123857 | Durablue Sterilization Wrap | Cardinal Health200, LLC | 2013 | — |
| −3 | K132060 | Durablue Sterilization Wrap | Cardinal Health-Medical Products and Services | 2013 | — |
| −2 | K151788 | Cardinal Health Sterilization Wrap | Cardinal Health200, LLC | 2015 | — |
| −1 | K181174 | Cardinal Health Sterilization Wrap | Cardinal Health200, LLC | 2018 | — |
| 0 (this device) | K233777 | PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600) | Primed Medical Products, Inc. | 2024 | — |
| +1 | K242208 | PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600) | Primed Medical Products, Inc. | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 1 | 0 |
| 2011 | 1 | 0 |
| 2012 | 2 | 0 |
| 2013 | 1 | 0 |
| 2015 | 1 | 0 |
| 2017 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2024 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in FRG? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new FRG device
- #1 K234050 HALYARD® ONE-STEP® Sterilization Wrap…score 15.8 · 7 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K181174 | Cardinal Health Sterilization WrapSummary page 8…FRG Predicate device(s) Cardinal Health Sterilization wrap K181174 Device Description: The PRIMED Sterilization wraps are made of SMS (Spunbond Meltblown Spunbond) Polypropylene with addition o… | 2018 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K242208 | PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600) | 2024 | 0 |
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 36 years and passes through 4 companies; a new generation was cleared every 1.9 years on median.
- 1 of the 17 ancestors has a recall of any class.
- Of its descendants, K242208 (Primed Medical Products, Inc., 2024) has gone furthest, with 0 descendants of its own.
- 1 other device also cites its predicate K181174.
How does its category compare?
All FRG devicesFRG Wrap, Sterilization: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.
FDA decisions per year · FRG
9in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FRG
151in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FRG
2in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FRG
18in 2025
MAUDE reports naming product code FRG, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 3 | 182 | 0 | 1 |
| 2008 | 2 | — | 0 | 2 |
| 2009 | 4 | 171 | 0 | 2 |
| 2010 | 4 | 213 | 0 | 0 |
| 2011 | 6 | 110 | 0 | 12 |
| 2012 | 10 | 133 | 0 | 4 |
| 2013 | 6 | 146 | 2 | 5 |
| 2014 | 8 | 177 | 0 | 13 |
| 2015 | 12 | 196 | 0 | 9 |
| 2016 | 9 | 131 | 0 | 20 |
| 2017 | 9 | 260 | 29 | 7 |
| 2018 | 5 | 150 | 0 | 22 |
| 2019 | 9 | 258 | 0 | 10 |
| 2020 | 5 | 122 | 14 | 21 |
| 2021 | 4 | 170 | 0 | 9 |
| 2022 | 9 | 217 | 2 | 4 |
| 2023 | 9 | 230 | 0 | 13 |
| 2024 | 11 | 182 | 0 | 21 |
| 2025 | 9 | 151 | 0 | 18 |
| 2026 | 4 | 247 | 0 | — |
What is it indicated for?
The PRIMED Sterilization wraps are intended to be used to enclose another medical device that is to be sterilized by a health care provider via the following: - Pre-Vacuum Steam at 270°F/ 132°C for 4 minutes. The wrap has been validated for dry time of 20 minutes for P100 and P200 and dry time of 30 minutes for P300, P400, P500 and P600. - 100% Ethylene Oxide Sterilization with a concentration of 725-735 mg/L at 131°F/55°C and 40% - 80% relative humidity…
Read the full statement (1,321 words)
The PRIMED Sterilization wraps are intended to be used to enclose another medical device that is to be sterilized by a health care provider via the following:
- Pre-Vacuum Steam at 270°F/ 132°C for 4 minutes. The wrap has been validated for dry time of 20 minutes for P100 and P200 and dry time of 30 minutes for P300, P400, P500 and P600.
- 100% Ethylene Oxide Sterilization with a concentration of 725-735 mg/L at 131°F/55°C and 40% - 80% relative humidity for 60 minutes. Validated for aeration times of 8 hours at 55°C or 12 hours at 43.3°C.
- Lumen, Non-Lumen, and Flexible Cycles in the STERIS V-PRO maX/maX2 and STERIS V-PRO 60/s2 low temperature Sterilization Systems.
- Advanced Sterilization Products STERRAD 100S system
- Advanced Sterilization Products STERRAD NX [Standard Cycle, Advanced Cycle]
- Advanced Sterilization Products STERRAD 100 NX [Standard Cycle, Flex Cycle, Express, Duo Cycle]
PRIMED Sterilization wraps are available in 6 models and different sizes ranging from 12" X 12" to 54" X 90" and are intended to allow sterilization of the enclosed medical device(s) and maintain sterility of the enclosed device(s) until used.
PRIMED Sterilization wraps are validated for use with above listed sterilization systems with the intended loads as described below.
PRIMED wraps are validated for Pre-Vacuum Steam and EO sterilization with two 3.0mm x 400 mm lumen devices as part of the load.
PRIMED wraps are validated for ASP STERRAD 100 S sterilization with 10 stainless steel lumens (2mm ID x 250 mm length) as part of their load.
PRIMED Sterilization wraps are validated for use with STERIS V-PRO cycles and intended load as listed below:
V- PRO maX/maX2 Non-Lumen Cycle:
• Non-lumened instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors.
• Non-lumened instruments including non-lumened general medical instruments, non-lumened rigid, semi-rigid and flexible endoscopes.
V- PRO maX/maX2 Lumen Cycle:
• Non-lumened instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors.
• Single, dual, or triple channeled stainless steel lumen that are:
o ≥ 0.77 mm ID and ≤ 527 mm in length.
o ≥ 0.8 mm ID and ≤ 542 mm in length.
o ≥0.48 mm ID and ≤ 100 mm in length .
• Dead end lumen that is ≥ 1.3 mm ID and ≤ 73 mm in length
• Rigid non-metallic lumen that are:
o ≥ 3 mm ID and ≤ 298 mm in length.
o ≥ 4 mm ID and ≤ 424 mm in length.
V- PRO maX/maX2 Flexible Cycle:
• Non-lumened instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors.
• Single or dual lumen surgical flexible endoscopes (such as those used in ENT, Urology and Surgical Care) and bronchoscopes in either of the two configurations:
o Two flexible endoscopes with a light cord (if not integral to endoscope) and mat with no additional load. The flexible endoscopes may contain:
- Single or dual channel lumens that are ≥ 1 mm ID and ≤ 1050 mm in length
o One flexible endoscope with a light cord (if not integral to the endoscope) and mat and additional instruments. The flexible endoscope may contain:
- Single or dual channel lumens that are ≥ 1 mm ID and ≤ 1050 mm in length
- Additional load, up to 24 lbs (11 kg) can include lumened or non-lumened medical devices:
- Single, dual, or triple channel stainless steel lumens ≥0.48 mm ID and ≤ 100 mm in length
V-PRO 60/s2 Non-Lumen Cycle:
• Non-lumened instruments and instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors.
• Non-lumened instruments including non-lumened general medical instruments, non-lumened rigid, semi-rigid and flexible endoscopes.
V- PRO 60/s2 Lumen Cycle:
• Non-lumened instruments and instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors.
• Medical devices (including single, dual, and triple channeled rigid and semi-rigid endoscopes) with the following configurations:
o Single or dual channeled devices with stainless steel lumens that are:
- ≥ 0.77 mm ID and ≤ 410 mm in length.
- ≥ 1.8 mm ID and ≤ 542 mm in length.
o Triple channeled devices with stainless steel lumens that are either:
- ≥1.2 mm ID and ≤275 mm in length
- ≥1.8 mm ID and ≤ 310 mm in length or
- ≥ 2.8 mm ID and ≤317 mm in length
V-PRO 60/s2 Flexible Cycle:
• Non-lumened instruments and instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors.
• One surgical flexible endoscope (such as those used in ENT, Urology and Surgical Care) or bronchoscope with light cord (if not integral to the endoscope), mat, and additional load.
o The flexible endoscope may be a single or dual lumen device with lumens that are ≥ 1 mm ID and ≤ 990 mm in length.
o Additional load, up to 11 lb (5 kg) can include stainless steel lumens with the following dimensions:
- ≥ 0.76 mm ID and ≤ 233 mm in length
- ≥ 1.0 mm ID and ≤ 254 mm in length
- ≥ 1.8 mm ID and ≤ 542 mm in length
The PRIMED Sterilization wraps are validated with ASP STERRAD 100 NX and ASP STERRAD NX and ASP STERRAD 100s sterilization cycles and intended load detailed below:
STERRAD 100NX Standard cycle:
• Instruments with diffusion-restricted spaces, such as the hinged portion of forceps and scissors.
• Single channel stainless steel lumens with an inside diameter of 0.7 mm or larger and a length of 500 mm or shorter. (A maximum of ten single channel stainless steel lumens, five per tray per sterilization cycle).
STERRAD 100NX Flex Cycle:
• Instruments with diffusion-restricted spaces, such as the hinged portion of forceps and scissors.
• Medical devices, including most flexible endoscopes, with the following materials and dimensions:
o Single channel polyethylene and Teflon (polytetrafluoroethylene) flexible endoscopes with an inside diameter of 1 mm or larger and length of 1065 mm or shorter. (A maximum of two flexible endoscopes, one per tray per sterilization cycle. No additional load)
STERRAD 100NX Express Cycle:
• Instruments surfaces and instruments having diffusion-restricted spaces, such as the hinged portion of forceps and scissors.
• Medical devices, including rigid or semi-rigid endoscopes without lumen.
STERRAD 100NX DUO Cycle:
• Instruments with diffusion-restricted spaces, such as the hinged portion of forceps and scissors.
• Medical devices, including most flexible endoscopes, with the following materials and dimensions:
o Single channel polyethylene and Teflon (polytetrafluoroethylene) flexible endoscopes with an inside diameter of 1 mm or larger and a length of 875 mm or shorter
o Accessory devices that are normally connected to a flexible endoscope during use.
o Flexible endoscopes without lumens
STERRAD NX Standard cycle:
• Instruments with diffusion-restricted spaces, such as the hinged portion of forceps and scissors and up to 10 lumens of followings.
o Single channel stainless steel lumens with an inside diameter of 1 mm or larger and a length of 150 mm or shorter
o Single-channel stainless steel lumens with an inside diameter of 2 mm or larger and a length of 400 mm or shorter
STERRAD NX Advanced Cycle:
• Instruments with diffusion-restricted spaces, such as the hinged portion of forceps and scissors.
• Single channel stainless steel lumens with an inside diameter of 1 mm or larger and a length of 500 mm or shorter (up to 10 Lumen per load)
• Single channel polyethylene and Teflon (polytetrafluoroethylene) flexible endoscope with an inside diameter of 1 mm or larger and length of 1065 mm or shorter (no additional load)
STERRAD 100s:
• Instruments with diffusion-restricted spaces, such as the hinged portion of forceps and scissors.
• Metal and nonmetal lumened instruments with inside diameter of 6 mm or larger and length of 310 mm or shorter.
• A single stainless steel lumen with an inside diameter of 3 mm or larger and a length of 400 mm or shorter.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K233777 · printed Nov 5, 2026
Cite this page
510(k) Report. “K233777: PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K233777
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026