510(k) Report

510(k) · Cleared

Cleared

Surgical Isolation Gown

K203415510(k) TraditionalCleared May 20, 2021182-day reviewClass II21 CFR 878.4040

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

Yanbian Pacific Textile Co., Ltd. · FYC Gown, Isolation, Surgical

Cleared on May 20, 2021 as substantially equivalent to K190306 (Amd Medicom, Inc., 2020) after a 182-day review. Its family tree reaches back 3 generations to 1995. 1 later device descends from it.

Decided
May 20, 2021
Review
182 days
Class
Class II
Product code
FYC
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K952116 (1995). 1 later device descends from it, 1 citing it directly.

  1. Root · 3 generations backK952116 Cover GownAmerican Threshold Industries, Inc. · 1995
  2. 2 generations backK160339 Cardinal Health Isolation GownCardinal Health200, LLC · 2016 · Recalled
  3. 1 generation backK190306 AMD Ritmed AssureWear VersaGownAmd Medicom, Inc. · 2020
  4. This deviceK203415 Surgical Isolation GownYanbian Pacific Textile Co., Ltd. · 2021
  5. Descendant · cites it directly · 0 of its ownK212422 Disposable Surgical Isolation GownCrown Name Disposable Hygiene Products Fty., Ltd. · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K212422Disposable Surgical Isolation GownCrown Name Disposable Hygiene Products Fty., Ltd. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K952116Cover GownAmerican Threshold Industries, Inc.1995—
−2K160339Cardinal Health Isolation GownCardinal Health200, LLC20162
−1K190306AMD Ritmed AssureWear VersaGownAmd Medicom, Inc.2020—
0 (this device)K203415Surgical Isolation GownYanbian Pacific Textile Co., Ltd.2021—
+1K212422Disposable Surgical Isolation GownCrown Name Disposable Hygiene Products Fty., Ltd.2022—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K203415, 1995–2022Source: 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 FYC? 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 FYC device

  1. #1 K190306 AMD Ritmed AssureWear VersaGownscore 14.0 · 2 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
*K190306AMD Ritmed AssureWear VersaGown
Summary page 5
…Product Code: FYC Regulation Number: 21 CFR 878.4040 4. Predicate Device 510K Number: K190306 - AMD Medicom Inc. Device Name: AMD Ritmed AssureWear™ VersaGown Cleared date:…
Amd Medicom, Inc.2020—

Also cleared against K190306: 4 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K212422Disposable Surgical Isolation GownCrown Name Disposable Hygiene Products Fty., Ltd.20220

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 4 companies; a new generation was cleared every 3.5 years on median.
  • 1 of the 3 ancestors has a recall of any class.
  • Of its descendants, K212422 (Crown Name Disposable Hygiene Products Fty., Ltd., 2022) has gone furthest, with 0 descendants of its own.
  • 4 other devices also cite its predicate K190306.

How does its category compare?

All FYC devices

FYC Gown, Isolation, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · FYC

1in 2024

2016: 22017: 12018: 12020: 12021: 72022: 102023: 42024: 1
2007high 10 (2022) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FYC

95in 2023

2021: 182 days median2022: 229 days median2023: 95 days median
2007high 229 (2022) · low 95 (2023)2026

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

Recalls per year · FYC

2in 2024

2024: 2
2007high 2 (2024) · low 0 (2007)2026

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

Adverse event reports per year · FYC

3in 2025

2007: 12008: 12010: 12012: 12013: 82014: 22019: 12020: 12023: 12024: 12025: 3
2007high 8 (2013) · low 0 (2009)2025

MAUDE reports naming product code FYC, 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
20070—01
20080—01
20090—00
20100—01
20110—00
20120—01
20130—08
20140—02
20150—00
20162—00
20171—00
20181—00
20190—01
20201—01
2021718200
20221022900
202349501
20241—21
20250—03
20260—0—

What is it indicated for?

The Surgical Isolation Gown is intended to protect patients and health care personnel from the transfer of microorganisms, body fluids and particulate material. Not intended for use in the operating room. In addition, the Surgical Isolation Gown meets the requirements of an AAMI Level 3 barrier protection for an isolation gown per ANSI/AAMI PB70:2012 Liquid Barrier Performance and Classification of Protective Apparel Drapes Intended for Use in Health Care Facilities (ANSI/AAMI PB70). The Surgical Isolation Gown is a single use, disposable medical device provided non-sterile.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K203415: Surgical Isolation Gown.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K203415

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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