510(k) Report

510(k) · Cleared

Cleared

Kimguard One Step Sterilization Wrap

K141712510(k) TraditionalCleared Dec 18, 2014176-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

Halyard Health · FRG Wrap, Sterilization

Cleared on Dec 18, 2014 as substantially equivalent to K112805 (Kimberly-Clark Corp., 2012) after a 176-day review. Its family tree reaches back 4 generations to 1988. 5 later devices descend from it.

Decided
Dec 18, 2014
Review
176 days
Class
Class II
Product code
FRG
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K881471 (1988). 5 ancestors in all. 5 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2009: 1 other ancestor2019: 1 descendant cleared2022: 1 descendant cleared2024: 1 descendant cleared2026: 2 descendants clearedK881471 · Kimguard (Regular & Heavy Duty) Sterile Wrap · Kimberly-Clark Corp. · 1988 · recalledK082177 · Kimguard One-Step Sterilization Wrap · Kimberly-Clark Corp. · 2009K091685 · Kimguard One-Step Sterilization Wrap, Models KC100, KC200, KC300, KC400, KC 500, KC600 · Kimberly-Clark Corp. · 2009K112805 · Kimguard One-Step Sterilization Wrap · Kimberly-Clark Corp. · 20121990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant3 generations forward: 1 descendant4 generations forward: 2 descendants K112805 · Kimguard One-Step Sterilization Wrap · Kimberly-Clark Corp. · 2012K091685 · Kimguard One-Step Sterilization Wrap, Models KC100, KC200, KC300, KC400, KC 500, KC600 · Kimberly-Clark Corp. · 2009K082177 · Kimguard One-Step Sterilization Wrap · Kimberly-Clark Corp. · 2009K881471 · Kimguard (Regular & Heavy Duty) Sterile Wrap · Kimberly-Clark Corp. · 1988 · recalled0
  1. Root · 4 generations backK881471 Kimguard (Regular & Heavy Duty) Sterile WrapKimberly-Clark Corp. · 1988 · Recalled
  2. 3 generations backK082177 Kimguard One-Step Sterilization WrapKimberly-Clark Corp. · 2009
  3. 2 generations backK091685 Kimguard One-Step Sterilization Wrap, Models KC100, KC200, KC300…Kimberly-Clark Corp. · 2009
  4. 1 generation backK112805 Kimguard One-Step Sterilization WrapKimberly-Clark Corp. · 2012
  5. This deviceK141712 Kimguard One Step Sterilization WrapHalyard Health · 2014
  6. Descendant · cites it directly · 4 of its ownK192147 Halyard ONE-STEP* Sterilization WrapOwens & Minor (O&M) Halyard, Inc. · 2019
  7. Descendant · 2 generations on · 3 of its ownK214007 HALYARD ONE-STEP Sterilization Wrap, HALYARD QUICK CHECK…Owens & Minor (O&M) Halyard, Inc. · 2022
  8. Descendant · 3 generations on · 2 of its ownK234050 HALYARD® ONE-STEP® Sterilization Wrap, HALYARD® QUICK CHECK®…O&M Halyard, Inc. · 2024
  9. Descendant · 4 generations on · 0 of its ownK261897 HALYARD* ARMOR-FLEX* Sterilization Wrap with ASSURE-DRY* Technology…O&M Halyard, Inc. · 2026
  10. Descendant · 4 generations on · 0 of its ownK253454 HALYARD* ONE-STEP* Sterilization Wrap; HALYARD* QUICK CHECK*…O&M Halyard, Inc. · 2026

Most influential descendants

Showing 5 of 5 · See all
  • K192147Halyard ONE-STEP* Sterilization WrapOwens & Minor (O&M) Halyard, Inc. · 2019 · cites it directly4descendants
  • K214007HALYARD ONE-STEP Sterilization Wrap, HALYARD QUICK CHECK Sterilization WrapOwens & Minor (O&M) Halyard, Inc. · 2022 · 2 generations on3descendants
  • K234050HALYARD® ONE-STEP® Sterilization Wrap, HALYARD® QUICK CHECK® Sterilization Wrap…O&M Halyard, Inc. · 2024 · 3 generations on2descendants
  • K261897HALYARD* ARMOR-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD*…O&M Halyard, Inc. · 2026 · 4 generations on0descendants
  • K253454HALYARD* ONE-STEP* Sterilization Wrap; HALYARD* QUICK CHECK* Sterilization Wrap…O&M Halyard, Inc. · 2026 · 4 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K881471Kimguard (Regular & Heavy Duty) Sterile WrapKimberly-Clark Corp.19881
−3K082177Kimguard One-Step Sterilization WrapKimberly-Clark Corp.2009—
−2K091685Kimguard One-Step Sterilization Wrap, Models KC100, KC200, KC300, KC400, KC…Kimberly-Clark Corp.2009—
−1K112805Kimguard One-Step Sterilization WrapKimberly-Clark Corp.2012—
0 (this device)K141712Kimguard One Step Sterilization WrapHalyard Health2014—
+1K192147Halyard ONE-STEP* Sterilization WrapOwens & Minor (O&M) Halyard, Inc.2019—
+2K214007HALYARD ONE-STEP Sterilization Wrap, HALYARD QUICK CHECK Sterilization WrapOwens & Minor (O&M) Halyard, Inc.2022—
+3K234050HALYARD® ONE-STEP® Sterilization Wrap, HALYARD® QUICK CHECK® Sterilization…O&M Halyard, Inc.2024—
+4K261897HALYARD* ARMOR-FLEX* Sterilization Wrap with ASSURE-DRY* Technology; HALYARD*…O&M Halyard, Inc.2026—
+4K253454HALYARD* ONE-STEP* Sterilization Wrap; HALYARD* QUICK CHECK* Sterilization…O&M Halyard, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
202210
202410
202620
FIG. 1 — Lineage of K141712, 1988–2026Source: 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
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K112805Kimguard One-Step Sterilization Wrap
Summary page 5
…SUAL NAME: Sterilization Wrap PRODUCT CODE: FRG DEVICE CLASSIFICATION: Class II per 21 CFR §880.6850 PREDICATE DEVICES: K112805 - KIMGUARD* ONE-STEP* Sterilization Wrap (Models KC100, KC200, KC300, KC400, KC500, and KC600).…
Kimberly-Clark Corp.2012—

Also cleared against K112805: 3 other devices →

What descends from it? (5)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K192147Halyard ONE-STEP* Sterilization WrapOwens & Minor (O&M) Halyard, Inc.20194

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 26 years and passes through 2 companies; a new generation was cleared every 2.8 years on median.
  • 1 of the 5 ancestors has a recall of any class.
  • Of its descendants, K192147 (Owens & Minor (O&M) Halyard, Inc., 2019) has gone furthest, with 4 descendants of its own.
  • 3 other devices also cite its predicate K112805.

How does its category compare?

All FRG devices

FRG Wrap, Sterilization: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, 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?

KIMGUARD ONE-STEP Sterilization Wraps are intended to enclose another medical device that is to be sterilized by a healthcare provider using: Sterilucent PSD-85 Hydrogen Peroxide Sterilizer that include: Lumen Cycle and Non-Lumen Cycle. KIMGUARD* ONE-STEP* Sterilization Wrap (KC100, KC200, KC300, KC400, KC500 and KC600) are intended to allow sterilization of the enclosed medical device(s) and also maintain sterility of the enclosed device(s) until used.…

Read the full statement (453 words)

KIMGUARD ONE-STEP Sterilization Wraps are intended to enclose another medical device that is to be sterilized by a healthcare provider using:

Sterilucent PSD-85 Hydrogen Peroxide Sterilizer that include:

Lumen Cycle and

Non-Lumen Cycle.

KIMGUARD* ONE-STEP* Sterilization Wrap (KC100, KC200, KC300, KC400, KC500 and KC600) are intended to allow sterilization of the enclosed medical device(s) and also maintain sterility of the enclosed device(s) until used.

Test results validated that KIMGUARD ONE-STEP Sterilization Wraps (KC100, KC200, KC300, KC400, KC500, and KC600) allowed sterilization of the enclosed devices by the Sterilucent PSD-85 Hydrogen Peroxide Sterilizer (i.e., both the Lumen and Non-Lumen Cycles). Additionally, the KIMGUARD ONE-STEP Sterilization Wrap was validated to allow effective aeration under the pre-programmed PSD-85 Sterilization Cycles.

The PSD-85 Lumen Cycle has been validated to sterilize a load of up to ten (10) pounds (combined pouch and wrapped tray load) containing a maximum of ten (10) single channel stainless steel lumens per load with the following dimensions:

• An inside diameter of 1 mm or larger and a length of 60 mm or shorter;

• An inside diameter of 2 mm or larger and a length of 250 mm or shorter;

• An inside diameter of 3 mm or larger and a length of 350 mm or shorter.

The PSD-85 Non-Lumen Cycle has been validated to sterilize a load of up to 25 pounds (combined pouch and wrapped tray load).

All models of the KIMGUARD ONE-STEP Sterilization Wrap (KC100, KC200, KC300, KC400, KC500, and KC600) have been validated for use with the Sterilucent PSD-85 Hydrogen Peroxide Sterilizer cycles in Table 1.

TABLE 1: Validated Sterilucent PSD-85 Hydrogen Peroxide Sterilizer Cycle

(Note: The instructions provided below are not intended to replace the detailed Instructions for Use provided with the Sterilucent PSD-85 Hydrogen Peroxide Sterilizer.)

PSD-85 Cycle — Intended Loads

Lumen: Reusable metal and nonmetal devices including devices with diffusion-restricted spaces such as the hinged portion of forceps and scissors and up to 10 single channel stainless steel lumened devices of the following dimensions per chamber load:

• An inside diameter of 1 mm or larger and a length of 60 mm or shorter

• An inside diameter of 2 mm or larger and a length of 250 mm or shorter

• An inside diameter of 3 mm or larger and a length of 350 mm or shorter

(Refer to the PSD-85 User Manual for complete instructions on load(s) and cycle(s), including chamber loading instructions (i.e. 10 lbs per load)

Non-Lumen: Non-lumened reusable metal and nonmetal devices including devices with stainless steel diffusion-restricted spaces such as the hinged portion of forceps and scissors.

(Refer to the PSD-85 User Manual for complete instructions on load(s) and cycle(s), including chamber loading instructions (i.e. 25 lbs per load))

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K141712: Kimguard One Step Sterilization Wrap.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141712

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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