510(k) Report

510(k) · Cleared

Cleared

DS N95 Surgical Masks and Flat Surgical

K090131510(k) AbbreviatedCleared Apr 27, 200996-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

Shanghai Dasheng Health Products · MSH Respirator, Surgical

Cleared on Apr 27, 2009 as substantially equivalent to K041855 (Aearo Co., 2004) and 2 other predicates after a 96-day review. Its family tree reaches back 3 generations to 1992.

Decided
Apr 27, 2009
Review
96 days
Class
Class II
Product code
MSH
Recalls
None
Predicates
3

Its longest line of descent runs back 3 generations to K922507 (1992). 5 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 3 generations backK922507 Gerson Isolair Apr Particulate Surgical MaskLouis M. Gerson Co., Inc. · 1992
  2. 2 generations backK960778 Isolair Apr Type N95Louis M. Gerson Co., Inc. · 1996
  3. 1 generation backK041855 Pleats Plus N95 Particulate Respirator, Models 1050 and 1050SAearo Co. · 2004
  4. This deviceK090131 DS N95 Surgical Masks and Flat SurgicalShanghai Dasheng Health Products · 2009
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K922507Gerson Isolair Apr Particulate Surgical MaskLouis M. Gerson Co., Inc.1992—
−2K960778Isolair Apr Type N95Louis M. Gerson Co., Inc.1996—
−1K041855Pleats Plus N95 Particulate Respirator, Models 1050 and 1050SAearo Co.2004—
0 (this device)K090131DS N95 Surgical Masks and Flat SurgicalShanghai Dasheng Health Products2009—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199710
200410
FIG. 1 — Lineage of K090131, 1992–2009Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 MSH? 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 MSH device

  1. #1 K233022 Halyard Fluidshield 3 N95 Particulate Filter…score 6.7 · 1 generation · no Class I recall
Get a 510(k) Report

What was it cleared against? (3)

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
*K041855Pleats Plus N95 Particulate Respirator, Models 1050 and 1050S
Summary page 2
…B and flat surgical masks color pink, blue, white, green, yellow, orange are substantially equivalent is safety and effectiveness to the predicate device. Aearo Company- K041855 Pleated plus 1050 and 1050S Gerson Isolair Compay -K960778 APR Type N95 model 2735 Tucker & Associates company-K022256 Surgical f…
Aearo Co.2004—
*K960778Isolair Apr Type N95
Summary page 2
…ellow, orange are substantially equivalent is safety and effectiveness to the predicate device. Aearo Company- K041855 Pleated plus 1050 and 1050S Gerson Isolair Compay -K960778 APR Type N95 model 2735 Tucker & Associates company-K022256 Surgical face masks white, yellow, pink, blue and green For reference…
Louis M. Gerson Co., Inc.1996—
*K022256Surgical Face Mask - Colors: White, Yellow, Pink, Blue, and Green
Summary page 2
…ectiveness to the predicate device. Aearo Company- K041855 Pleated plus 1050 and 1050S Gerson Isolair Compay -K960778 APR Type N95 model 2735 Tucker & Associates company-K022256 Surgical face masks white, yellow, pink, blue and green For reference: FXX, 878,4040. Class II Manufacturer…
Tucker & Associates2004—

Also cleared against K041855: 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 17 years and passes through 3 companies; a new generation was cleared every 4.5 years on median.
  • None of the 5 ancestors has a recall.
  • 4 other devices also cite its predicate K041855.

How does its category compare?

All MSH devices

MSH Respirator, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · MSH

1in 2024

2007: 72008: 22009: 22010: 42013: 12015: 12016: 12017: 12018: 12024: 1
2007high 7 (2007) · low 0 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MSH

60in 2010

2007: 78 days median2010: 60 days median
2007high 78 (2007) · low 60 (2010)2026

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

Recalls per year · MSH

1in 2008

2008: 1
2007high 1 (2008) · low 0 (2007)2026

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

Adverse event reports per year · MSH

10in 2025

2010: 22015: 32017: 22018: 42020: 592021: 192022: 182023: 712024: 12025: 10
2007high 71 (2023) · low 0 (2007)2025

MAUDE reports naming product code MSH, 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
200777800
20082—10
20092—00
201046002
20110—00
20120—00
20131—00
20140—00
20151—03
20161—00
20171—02
20181—04
20190—00
20200—059
20210—019
20220—018
20230—071
20241—01
20250—010
20260—0—

What is it indicated for?

The DS N95 Surgical Masks DTC3M-1/DTC3B, and flat surgical masks are intended for single use by operating room personnel and other health care workers to protect both the patients and the health care workers from transfer of microorganisms, blood fnd body fluids, and airborne particulate materials.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K090131: DS N95 Surgical Masks and Flat Surgical.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K090131

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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