510(k) · Cleared
ClearedPMSSteripack Flat Sterilization Pouch (FP) and Roll (FL) with Chemical Indicator
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Pms Tibbi Cihazlar Teknolojisi San VE Tic AS · FRG Wrap, Sterilization
Cleared on Oct 13, 2017 as substantially equivalent to K102158 (Sigma Medical Supplies Corp., 2011) after a 416-day review. Its family tree reaches back 5 generations to 1999.
- Decided
- Oct 13, 2017
- Review
- 416 days
- Class
- Class II
- Product code
- FRG
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 5 generations to K990567 (1999). No later device cites it as a predicate yet.
- Root · 5 generations backK990567 Global Healthcare Self-Sealing Sterilization PouchGlobal Healthcare, Inc. · 1999
- 4 generations backK993764 Medipack See-Through Seal Sterilization PouchMedipack Medical Packaging Mfg. Co. · 1999
- 3 generations backK051242 Winner Self Seal Sterilization PouchWinner Medical (Usa), Inc. · 2005
- 2 generations backK070428 Medicom Self-Sealing Sterilization PouchA.R. Medicom, Inc. · 2007
- 1 generation backK102158 Sigma Sterilization Pouch & RollSigma Medical Supplies Corp. · 2011
- This deviceK162362 PMSSteripack Flat Sterilization Pouch (FP) and Roll (FL) with…Pms Tibbi Cihazlar Teknolojisi San VE Tic AS · 2017
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K990567 | Global Healthcare Self-Sealing Sterilization Pouch | Global Healthcare, Inc. | 1999 | — |
| −4 | K993764 | Medipack See-Through Seal Sterilization Pouch | Medipack Medical Packaging Mfg. Co. | 1999 | — |
| −3 | K051242 | Winner Self Seal Sterilization Pouch | Winner Medical (Usa), Inc. | 2005 | — |
| −2 | K070428 | Medicom Self-Sealing Sterilization Pouch | A.R. Medicom, Inc. | 2007 | — |
| −1 | K102158 | Sigma Sterilization Pouch & Roll | Sigma Medical Supplies Corp. | 2011 | — |
| 0 (this device) | K162362 | PMSSteripack Flat Sterilization Pouch (FP) and Roll (FL) with Chemical Indicator | Pms Tibbi Cihazlar Teknolojisi San VE Tic AS | 2017 | — |
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 |
|---|---|---|---|
| * | K102158 | Sigma Sterilization Pouch & RollSummary page 6…cator, Physical/Chemical Sterilization Process Product Code: FRG – JOJ Product Classification: Class II 21 CFR 880.6850, General Hospital 3. Predicate Device K102158, SIGMA Sterilization Pouch and Roll 4. Indications For Use PMSSteripack Flat Sterilization Pouch (FP) and Roll (FL) with Chem… | 2011 |
What descends from it?
No later submission names this one as a predicate yet.
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 18 years and passes through 6 companies; a new generation was cleared every 4.0 years on median.
- None of the 5 ancestors has a recall.
- 4 other devices also cite its predicate K102158.
How does its category compare?
All FRG devicesFRG Wrap, Sterilization: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, 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?
PMSSteripack Flat Sterilization Pouch (FP) and Roll (FL) with Chemical Indicator, is a device intended to be used to enclose another medical device that is to be sterilized by a health care provider. It is intended to allow sterilization of the enclosed medical device and also to maintain sterility of the enclosed device until used. The recommended (and validated) sterilization cycle parameters for all models (Sterilization Pouches (FP) and Rolls(FL)…
Read the full statement (299 words)
PMSSteripack Flat Sterilization Pouch (FP) and Roll (FL) with Chemical Indicator, is a device intended to be used to enclose another medical device that is to be sterilized by a health care provider. It is intended to allow sterilization of the enclosed medical device and also to maintain sterility of the enclosed device until used.
The recommended (and validated) sterilization cycle parameters for all models (Sterilization Pouches (FP) and Rolls(FL) with Chemical Indicator) are;
For steam sterilization pre-vacuum cycle at 132 degrees C for 4 minutes. Validated minimum dry time is 20 minutes.
For EO sterilization; 100%ethylene oxide(EO) with a concentration of 725mg/l at 55 degrees C and 50-80%relative humidity for 60 minutes. Aeration time is 8 hours.
Chemical process indicators on the exterior of the pouch and roll indicate by color change that the pouch has undergone either a steam or ethylene oxide sterilization process.
Type1 steam indicator will change color from pink to brown after exposure to pre-vacuum steam sterilization process.
Type 1 ethylene oxide indicator will change from turquoise to yellow after exposure to ethylene oxide sterilization process.
As Worst Case Validated Load; general medical devices of stainless steel and devices with stainless steel lumens with the following internal diameter (ID) and Maximum Load weight and Maximum Lumen length can be processed in the validated steam and ETO sterilization cycles as follows;
Table 1.Worst Case Validated Load and Lumen Claims.
Pouch Size Product Code Max.Load Weight (lbs.) Max. lumen length (mm) Min. internal diameter (mm) Max # Lumens
50 x 200 mm FP 0520 0.062 50.8 mm 1.5 mm 1
200 x 300 mm FP 2030 0.516 200 mm 3.0 mm 1
250 x 300 mm FP 2530 0.520 200 mm 3.0 mm 1
500 x 600 mm FP 5060 3.344 400 mm 3.0 mm 1
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K162362 · printed Nov 6, 2026
Cite this page
510(k) Report. “K162362: PMSSteripack Flat Sterilization Pouch (FP) and Roll (FL) with Chemical Indicator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K162362
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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