510(k) Report

510(k) · Cleared

Cleared

Disposable Medical Surgical Face Mask

K203200510(k) TraditionalCleared Jun 16, 2021230-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

Guangdong Haiou Medical Apparatus Co., Ltd. · FXX Mask, Surgical

Cleared on Jun 16, 2021 as substantially equivalent to K201137 (Pfm Medical, Inc., 2020) after a 230-day review. Its family tree reaches back 8 generations to 1987. 1 later device descends from it.

Decided
Jun 16, 2021
Review
230 days
Class
Class II
Product code
FXX
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K874608 (1987). 11 ancestors in all, the oldest K801036 (1980). 1 later device descends from it, 1 citing it directly.

  1. Root · 8 generations backK874608 Tecnol Fluid Shield Surgical MaskTecnol New Jersey Wound Care, Inc. · 1987
  2. 7 generations backK955556 Fluid Resistant MaskAmerican Threshold Healthcare · 1996
  3. 6 generations backK012602 Crosstex Isolite Earloop Face Masks-Blue, Pink, Crosstex Isofluid…Crosstex Intl. · 2002
  4. 5 generations backK040333 Valumax Surgical Masks (Blue, Pink, Green, Yellow, White and Peach)…Valumax Intl., Inc. · 2004
  5. 4 generations backK051291 Non-Sterile Surgical MaskA.R. Medicom, Inc. · 2005 · Recalled
  6. 3 generations backK061864 Dukal Surgical Face Mask Tie-on, Model 1530; Ear Loop, Model 1540…Dukal Corp. · 2006
  7. 2 generations backK111559 Surgical MasksShanghai Neo-Medical Import & Export Co., Ltd. · 2011
  8. 1 generation backK201137 Asept Surgical Face MaskPfm Medical, Inc. · 2020
  9. This deviceK203200 Disposable Medical Surgical Face MaskGuangdong Haiou Medical Apparatus Co., Ltd. · 2021
  10. Descendant · cites it directly · 0 of its ownK210643 Disposable Surgical Face MaskShandong Zhushi Pharmaceutical Group Co., Ltd. · 2021

Most influential descendants

Showing 1 of 1 · See all
  • K210643Disposable Surgical Face MaskShandong Zhushi Pharmaceutical Group Co., Ltd. · 2021 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K874608Tecnol Fluid Shield Surgical MaskTecnol New Jersey Wound Care, Inc.1987—
−7K955556Fluid Resistant MaskAmerican Threshold Healthcare1996—
−6K012602Crosstex Isolite Earloop Face Masks-Blue, Pink, Crosstex Isofluid Earloop Face…Crosstex Intl.2002—
−5K040333Valumax Surgical Masks (Blue, Pink, Green, Yellow, White and Peach) with or…Valumax Intl., Inc.2004—
−4K051291Non-Sterile Surgical MaskA.R. Medicom, Inc.20055
−3K061864Dukal Surgical Face Mask Tie-on, Model 1530; Ear Loop, Model 1540; with…Dukal Corp.2006—
−2K111559Surgical MasksShanghai Neo-Medical Import & Export Co., Ltd.2011—
−1K201137Asept Surgical Face MaskPfm Medical, Inc.2020—
0 (this device)K203200Disposable Medical Surgical Face MaskGuangdong Haiou Medical Apparatus Co., Ltd.2021—
+1K210643Disposable Surgical Face MaskShandong Zhushi Pharmaceutical Group Co., Ltd.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
199110
199610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
FIG. 1 — Lineage of K203200, 1987–2021Source: 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 FXX? 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 FXX device

  1. #1 K201479 DemeMASKscore 40.2 · 6 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
*K201137Asept Surgical Face Mask
Summary page 5
…el: General Hospital 4. Predicate Device Information: Page 1 of 7 510(k) Summary  510(k) Number: K201137  Predicate Device Name: ASEPT® Surgical Face Mask  Manufacturer: PFM Medical, Inc.  This predicate has not been su…
Pfm Medical, Inc.2020—

Also cleared against K201137: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K210643Disposable Surgical Face MaskShandong Zhushi Pharmaceutical Group Co., Ltd.20210

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 34 years and passes through 9 companies; a new generation was cleared every 5.0 years on median.
  • 2 of the 11 ancestors have a recall of any class.
  • Of its descendants, K210643 (Shandong Zhushi Pharmaceutical Group Co., Ltd., 2021) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K201137.

How does its category compare?

All FXX devices

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

FDA decisions per year · FXX

6in 2025

2007: 22008: 22009: 12010: 72011: 62012: 12013: 32014: 12015: 52016: 52017: 12018: 32019: 42020: 272021: 2182022: 912023: 222024: 152025: 62026 (partial year): 5
2007high 218 (2021) · low 1 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FXX

123in 2025

2010: 144 days median2011: 137 days median2013: 219 days median2015: 298 days median2016: 268 days median2018: 119 days median2019: 124 days median2020: 113 days median2021: 162 days median2022: 113 days median2023: 139 days median2024: 263 days median2025: 123 days median2026 (partial year): 142 days median
2007high 298 (2015) · low 113 (2020)2026

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

Recalls per year · FXX

2in 2024

2019: 22023: 12024: 2
2007high 2 (2019) · low 0 (2007)2026

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

Adverse event reports per year · FXX

11in 2025

2007: 112008: 102009: 32010: 92011: 82012: 222013: 92014: 52015: 142016: 162017: 452018: 212019: 232020: 602021: 672022: 212023: 212024: 212025: 11
2007high 67 (2021) · low 3 (2009)2025

MAUDE reports naming product code FXX, 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
20072—011
20082—010
20091—03
2010714409
2011613708
20121—022
2013321909
20141—05
20155298014
20165268016
20171—045
20183119021
20194124223
202027113060
2021218162067
202291113021
202322139121
202415263221
20256123011
202651420—

What is it indicated for?

Disposable Medical Surgical Face Mask is indicated as a protective nose and mouth covering for healthcare workers and patients involved in medical and surgical procedures. The masks are indicated in any procedure or situation where there is a risk of exposure to microorganisms and body fluids.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K203200: Disposable Medical Surgical Face Mask.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K203200

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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