510(k) Report

510(k) · Cleared

Cleared

Gerson Isolair Apr Particulate Surgical Mask

K922507510(k) TraditionalCleared Nov 16, 1992173-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

Louis M. Gerson Co., Inc. · FXX Mask, Surgical

Cleared on Nov 16, 1992 after a 173-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 22 later devices descend from it.

Decided
Nov 16, 1992
Review
173 days
Class
Class II
Product code
FXX
Recalls
None
Predicates
0

22 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 1996: 1 descendant cleared2002: 1 descendant cleared2010: 4 descendants cleared2005: 1 descendant cleared1997: 1 descendant cleared2007: 5 descendants cleared2009: 2 descendants cleared2008: 2 descendants cleared2004: 1 descendant cleared2006: 3 descendants cleared2015: 1 descendant cleared1990200020102020
  1. This deviceK922507 Gerson Isolair Apr Particulate Surgical MaskLouis M. Gerson Co., Inc. · 1992
  2. Descendant · cites it directly · 21 of its ownK960778 Isolair Apr Type N95Louis M. Gerson Co., Inc. · 1996
  3. Descendant · 2 generations on · 15 of its ownK041855 Pleats Plus N95 Particulate Respirator, Models 1050 and 1050SAearo Co. · 2004
  4. Descendant · 2 generations on · 11 of its ownK051182 Inovel Health Care Model N95 Particulate Respirators and Surgical…Inovel, LLC · 2005 · Recalled
  5. Descendant · 3 generations on · 5 of its ownK070139 Willson One-Fit Healthcare Particle Respirator and Surgical Mask…Survivair, Inc. · 2007
  6. Descendant · 4 generations on · 3 of its ownK070782 Willson One-Fit Flat-Fold Healthcare Particulate Respirator and…Survivair Respirators, LLC · 2007

Showing 5 of 22 descendants. See all descendants

Descendants cleared per year

1996: 11997: 12002: 12004: 12005: 12006: 32007: 52008: 22009: 22010: 42015: 1
1996high 5 (2007) · low 0 (1998)2026

Most influential descendants

Showing 5 of 22 · See all
  • K960778Isolair Apr Type N95Louis M. Gerson Co., Inc. · 1996 · cites it directly21descendants
  • K041855Pleats Plus N95 Particulate Respirator, Models 1050 and 1050SAearo Co. · 2004 · 2 generations on15descendants
  • K051182Inovel Health Care Model N95 Particulate Respirators and Surgical MasksInovel, LLC · 2005 · 2 generations on11descendants
  • K070139Willson One-Fit Healthcare Particle Respirator and Surgical Mask, HC-NB095Survivair, Inc. · 2007 · 3 generations on5descendants
  • K070782Willson One-Fit Flat-Fold Healthcare Particulate Respirator and Surgical Mask, Models…Survivair Respirators, LLC · 2007 · 4 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K922507Gerson Isolair Apr Particulate Surgical MaskLouis M. Gerson Co., Inc.1992—
+1K960778Isolair Apr Type N95Louis M. Gerson Co., Inc.1996—
+2K041855Pleats Plus N95 Particulate Respirator, Models 1050 and 1050SAearo Co.2004—
+2K051182Inovel Health Care Model N95 Particulate Respirators and Surgical MasksInovel, LLC20051
+3K070139Willson One-Fit Healthcare Particle Respirator and Surgical Mask, HC-NB095Survivair, Inc.2007—
+4K070782Willson One-Fit Flat-Fold Healthcare Particulate Respirator and Surgical Mask…Survivair Respirators, LLC2007—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
199710
200210
200410
200510
200630
200750
200820
200920
201040
201510
FIG. 1 — Lineage of K922507, 1992–2015Source: 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), 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?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (22)

See all 22

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

NumberDeviceApplicantDecidedDescendants
K960778Isolair Apr Type N95Louis M. Gerson Co., Inc.199621

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?

  • Of its descendants, K960778 (Louis M. Gerson Co., Inc., 1996) has gone furthest, with 21 descendants of its own.

How does its category compare?

All FXX devices

FXX Mask, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years.

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—
Cite this page

510(k) Report. “K922507: Gerson Isolair Apr Particulate Surgical Mask.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K922507

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026