510(k) Report

510(k) · Cleared

Cleared

PMSSteripack Flat Sterilization Pouch (FP) and Roll (FL) with Chemical Indicator

K162362510(k) TraditionalCleared Oct 13, 2017416-day reviewClass II21 CFR 880.6850

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

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.

  1. Root · 5 generations backK990567 Global Healthcare Self-Sealing Sterilization PouchGlobal Healthcare, Inc. · 1999
  2. 4 generations backK993764 Medipack See-Through Seal Sterilization PouchMedipack Medical Packaging Mfg. Co. · 1999
  3. 3 generations backK051242 Winner Self Seal Sterilization PouchWinner Medical (Usa), Inc. · 2005
  4. 2 generations backK070428 Medicom Self-Sealing Sterilization PouchA.R. Medicom, Inc. · 2007
  5. 1 generation backK102158 Sigma Sterilization Pouch & RollSigma Medical Supplies Corp. · 2011
  6. 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

GenerationNumberDeviceApplicantDecidedRecalls
−5K990567Global Healthcare Self-Sealing Sterilization PouchGlobal Healthcare, Inc.1999—
−4K993764Medipack See-Through Seal Sterilization PouchMedipack Medical Packaging Mfg. Co.1999—
−3K051242Winner Self Seal Sterilization PouchWinner Medical (Usa), Inc.2005—
−2K070428Medicom Self-Sealing Sterilization PouchA.R. Medicom, Inc.2007—
−1K102158Sigma Sterilization Pouch & RollSigma Medical Supplies Corp.2011—
0 (this device)K162362PMSSteripack Flat Sterilization Pouch (FP) and Roll (FL) with Chemical IndicatorPms Tibbi Cihazlar Teknolojisi San VE Tic AS2017—
FIG. 1 — Lineage of K162362, 1999–2017Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K234050 HALYARD® ONE-STEP® Sterilization Wrap…score 15.8 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K102158Sigma Sterilization Pouch & Roll
Summary 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…
Sigma Medical Supplies Corp.2011—

Also cleared against K102158: 4 other devices →

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 devices

FRG 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

2007: 32008: 22009: 42010: 42011: 62012: 102013: 62014: 82015: 122016: 92017: 92018: 52019: 92020: 52021: 42022: 92023: 92024: 112025: 92026 (partial year): 4
2007high 12 (2015) · low 2 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FRG

151in 2025

2007: 182 days median2009: 171 days median2010: 213 days median2011: 110 days median2012: 133 days median2013: 146 days median2014: 177 days median2015: 196 days median2016: 131 days median2017: 260 days median2018: 150 days median2019: 258 days median2020: 122 days median2021: 170 days median2022: 217 days median2023: 230 days median2024: 182 days median2025: 151 days median2026 (partial year): 247 days median
2007high 260 (2017) · low 110 (2011)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FRG

2in 2022

2013: 22017: 292020: 142022: 2
2007high 29 (2017) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · FRG

18in 2025

2007: 12008: 22009: 22011: 122012: 42013: 52014: 132015: 92016: 202017: 72018: 222019: 102020: 212021: 92022: 42023: 132024: 212025: 18
2007high 22 (2018) · low 0 (2010)2025

MAUDE reports naming product code FRG, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007318201
20082—02
2009417102
2010421300
20116110012
20121013304
2013614625
20148177013
20151219609
20169131020
20179260297
20185150022
20199258010
202051221421
2021417009
2022921724
20239230013
202411182021
20259151018
202642470—

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.

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