510(k) · Cleared
ClearedVis-U-All Low Temperature Sterilization Pouch/Tubing
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
STERIS Corporation · FRG Wrap, Sterilization
Cleared on Jul 22, 2016 as substantially equivalent to K140487 (STERIS Corporation, 2014) after a 112-day review. Its family tree reaches back 4 generations to 1977. 6 later devices descend from it.
- Decided
- Jul 22, 2016
- Review
- 112 days
- Class
- Class II
- Product code
- FRG
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K771032 (1977). 7 ancestors in all. 6 later devices descend from it, 1 citing it directly.
- Root · 4 generations backK771032 Pouches, Peel Open, BreathableSurgicot, Inc. · 1977
- 3 generations backK070765 Vis-U-All II Self Seal PouchSTERIS Corporation · 2007
- 2 generations backK090371 Vis-U-All Low Temperature Tyvek Sterilization Pouch for V-Pro 1…STERIS Corporation · 2009
- 1 generation backK140487 Vis-U-All Low Temperature Sterilization Pouch/TubingSTERIS Corporation · 2014
- This deviceK160908 Vis-U-All Low Temperature Sterilization Pouch/TubingSTERIS Corporation · 2016
- Descendant · cites it directly · 5 of its ownK172749 Vis-U-All Low Temperature Sterilization Pouch/TubingSTERIS Corporation · 2018
- Descendant · 2 generations on · 3 of its ownK183401 Vis-U-All Low Temperature Sterilization Pouch/TubingSTERIS Corporation · 2019
- Descendant · 3 generations on · 2 of its ownK222440 Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE…Steris · 2022
- Descendant · 4 generations on · 0 of its ownK231501 PRO-LITE Sterilization TraySTERIS Corporation · 2023
- Descendant · 4 generations on · 0 of its ownK231500 Vis-U-All Low Temperature Sterilization PouchesSTERIS Corporation · 2023
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K172749Vis-U-All Low Temperature Sterilization Pouch/TubingSTERIS Corporation · 2018 · cites it directly5descendants
- K183401Vis-U-All Low Temperature Sterilization Pouch/TubingSTERIS Corporation · 2019 · 2 generations on3descendants
- K222440Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization TraysSteris · 2022 · 3 generations on2descendants
- K231501PRO-LITE Sterilization TraySTERIS Corporation · 2023 · 4 generations on0descendants
- K231500Vis-U-All Low Temperature Sterilization PouchesSTERIS Corporation · 2023 · 4 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K771032 | Pouches, Peel Open, Breathable | Surgicot, Inc. | 1977 | — |
| −3 | K070765 | Vis-U-All II Self Seal Pouch | STERIS Corporation | 2007 | — |
| −2 | K090371 | Vis-U-All Low Temperature Tyvek Sterilization Pouch for V-Pro 1 Sterilization… | STERIS Corporation | 2009 | — |
| −1 | K140487 | Vis-U-All Low Temperature Sterilization Pouch/Tubing | STERIS Corporation | 2014 | — |
| 0 (this device) | K160908 | Vis-U-All Low Temperature Sterilization Pouch/Tubing | STERIS Corporation | 2016 | — |
| +1 | K172749 | Vis-U-All Low Temperature Sterilization Pouch/Tubing | STERIS Corporation | 2018 | — |
| +2 | K183401 | Vis-U-All Low Temperature Sterilization Pouch/Tubing | STERIS Corporation | 2019 | — |
| +3 | K222440 | Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization… | Steris | 2022 | — |
| +4 | K231501 | PRO-LITE Sterilization Tray | STERIS Corporation | 2023 | — |
| +4 | K231500 | Vis-U-All Low Temperature Sterilization Pouches | STERIS Corporation | 2023 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1982 | 1 | 0 |
| 1995 | 1 | 0 |
| 2007 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 1 | 0 |
| 2019 | 2 | 0 |
| 2022 | 1 | 0 |
| 2023 | 2 | 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 |
|---|---|---|---|
| * | K140487 | Vis-U-All Low Temperature Sterilization Pouch/TubingSummary page 6…ion wrap (21 CFR 880.6850, Product Code FRG). 2. Predicate Device Vis-U-All Low Temperature Sterilization Pouch/Tubing (K140487) Reference Device - Vis-U-All Low Temperature Sterilization Pouch/Tubing (K092745) 3. Description of Device… | 2014 |
| † | K092745 | Vis-U-All Low Temperature Tyvek Sterilization Pouch for Ethylene Oxide, Models: Self and… | 2010 |
What descends from it? (6)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K172749 | Vis-U-All Low Temperature Sterilization Pouch/Tubing | 2018 | 5 |
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 39 years and passes through 2 companies; a new generation was cleared every 5.2 years on median.
- 1 of the 7 ancestors has a recall of any class.
- Of its descendants, K172749 (STERIS Corporation, 2018) has gone furthest, with 5 descendants of its own.
- 1 other device also cites its predicate K140487.
How does its category compare?
All FRG devicesFRG Wrap, Sterilization: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, 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 Vis-U-All Low Temperature Sterilization Pouches/Tubing are sterilization containment pouches for use by health care providers to enclose: • medical devices in a single or double pouch configuration • trays* containing medical devices in a single or double pouch configuration • small items requiring surface sterilization in a single pouch configuration within a tray* to be sterilized in the Lumen, Non Lumen and Flexible Cycles of the V-PRO Low…
Read the full statement (630 words)
The Vis-U-All Low Temperature Sterilization Pouches/Tubing are sterilization containment pouches for use by health care providers to enclose:
• medical devices in a single or double pouch configuration
• trays* containing medical devices in a single or double pouch configuration
• small items requiring surface sterilization in a single pouch configuration within a tray*
to be sterilized in the Lumen, Non Lumen and Flexible Cycles of the V-PRO Low Temperature Sterilization Systems. The pouches maintain the sterility of the enclosed devices until used.
When used to enclose medical devices, the pouches are intended to contain the devices in such a manner as to leave a minimum of one inch between the devices and seal on all sides. When used to enclose a tray, the tray must fit loosely within the pouch.
Vis-U-All Pouch/Tubing Claims with V-PRO Sterilization Systems
Intended Pouch Load when Medical Devices are:
• Directly Pouched or
• Placed Inside of a Tray* and the Tray* Pouched
V-PRO 60 Lumen Cycle
• Instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors
• Non-lumened devices including non-lumened rigid and semi-rigid endoscopes
• Medical devices, including single, dual and triple channeled rigid and semi-rigid endoscopes, with the following configurations:
o single or dual lumen devices
▪ ≥ 0.77 mm ID and ≤ 410 mm in length
o triple lumen devices
▪ ≥ 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 Non Lumen Cycle
Non-lumened devices including non-lumened rigid, semi-rigid and flexible endoscopes and non-lumened devices with stainless steel or titanium diffusion-restricted spaces such as the hinged portion of forceps and scissors.
V-PRO 60 Flexible Cycle
One flexible surgical endoscope or bronchoscope with a light cord (if not integral to endoscope) and mat without any additional load. The flexible endoscope may be a single or dual lumen device with lumens that are > 1 mm ID and < 990 mm in length
V-PRO 1, 1 Plus & maX Lumen Cycle
• Instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors
• Non-lumened devices including non-lumened rigid and semi-rigid endoscopes
• Medical devices, including single, dual and triple channeled rigid and semi-rigid endoscopes, with the following configurations:
o single or dual lumen devices
▪ ≥ 0.77 mm ID and ≤ 527 mm in length
o triple lumen devices
▪ ≥ 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 1 Plus & maX Non Lumen Cycle
Non-lumened devices including non-lumened rigid, semi-rigid and flexible endoscopes and non-lumened devices with stainless steel diffusion-restricted spaces such as the hinged portion of forceps and scissors.
V-PRO maX Flexible Cycle
Load 1: Single or dual lumen surgical flexible endoscopes (such as those used in ENT, Urology and Surgical Care) and bronchoscopes with a light cord (if not integral to endoscope) and mat with no additional load.
The flexible endoscopes may contain either:
• a single lumen that is > 1 mm ID and < 1050 mm in length
• or two lumens with:
• one lumen that is > 1 mm ID and < 990 mm in length
• and the other lumen that is > 1 mm ID and < 850 mm in length
Load 2: Non-lumened instruments including instruments with diffusion-restricted areas such as the hinged portion of forceps or scissors.
*Trays must be legally marketed for use in the V-PRO Low Temperature Sterilization Systems and contain a vent surface area to tray volume ratio ≥ 0.135 in-1 with the maximum number of instrument organizers installed.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K160908 · printed Nov 4, 2026
Cite this page
510(k) Report. “K160908: Vis-U-All Low Temperature Sterilization Pouch/Tubing.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K160908
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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