510(k) Report

510(k) · Cleared

Cleared

Mobilaire Iii and V Model Irc 301 and 501 Oxy. Con

K904087510(k) TraditionalCleared Oct 26, 199052-day reviewClass II21 CFR 868.5440

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

Invacare Corp. · CAW Generator, Oxygen, Portable

Cleared on Oct 26, 1990 after a 52-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 19 later devices descend from it.

Decided
Oct 26, 1990
Review
52 days
Class
Class II
Product code
CAW
Recalls
None
Predicates
0

19 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2002: 6 descendants cleared2001: 1 descendant cleared2006: 1 descendant cleared2014: 1 descendant cleared2004: 3 descendants cleared2008: 1 descendant cleared2007: 3 descendants cleared2011: 2 descendants cleared2010: 1 descendant cleared1990200020102020
  1. This deviceK904087 Mobilaire Iii and V Model Irc 301 and 501 Oxy. ConInvacare Corp. · 1990
  2. Descendant · cites it directly · 16 of its ownK011844 Merits Health Products Oxygen ConcentratorsMerits Health Products., Inc. · 2001
  3. Descendant · 2 generations on · 13 of its ownK014078 ON Site Gas Systems Portable Oxygen Generator SystemOn Site Gas Systems, Inc. · 2002
  4. Descendant · 2 generations on · 6 of its ownK020362 P.O.G.S. 3.3 Portable Oxygen Generator SystemOn Site Gas Systems, Inc. · 2002
  5. Descendant · 3 generations on · 5 of its ownK020330 Deployable Oxygen Concentration System (Docs)Pacific Consolidated Industries Llp · 2002
  6. Descendant · 3 generations on · 4 of its ownK030920 POGS 33On Site Gas Systems, Inc. · 2004

Showing 5 of 19 descendants. See all descendants

Descendants cleared per year

2001: 12002: 62004: 32006: 12007: 32008: 12010: 12011: 22014: 1
2001high 6 (2002) · low 0 (2003)2026

Most influential descendants

Showing 5 of 19 · See all
  • K011844Merits Health Products Oxygen ConcentratorsMerits Health Products., Inc. · 2001 · cites it directly16descendants
  • K014078ON Site Gas Systems Portable Oxygen Generator SystemOn Site Gas Systems, Inc. · 2002 · 2 generations on13descendants
  • K020362P.O.G.S. 3.3 Portable Oxygen Generator SystemOn Site Gas Systems, Inc. · 2002 · 2 generations on6descendants
  • K020330Deployable Oxygen Concentration System (Docs)Pacific Consolidated Industries Llp · 2002 · 3 generations on5descendants
  • K030920POGS 33On Site Gas Systems, Inc. · 2004 · 3 generations on4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K904087Mobilaire Iii and V Model Irc 301 and 501 Oxy. ConInvacare Corp.1990—
+1K011844Merits Health Products Oxygen ConcentratorsMerits Health Products., Inc.2001—
+2K014078ON Site Gas Systems Portable Oxygen Generator SystemOn Site Gas Systems, Inc.2002—
+2K020362P.O.G.S. 3.3 Portable Oxygen Generator SystemOn Site Gas Systems, Inc.2002—
+3K020330Deployable Oxygen Concentration System (Docs)Pacific Consolidated Industries Llp2002—
+3K030920POGS 33On Site Gas Systems, Inc.2004—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200110
200260
200430
200610
200730
200810
201010
201120
201410
FIG. 1 — Lineage of K904087, 1990–2014Source: 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 CAW? 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 CAW device

  1. #1 K230052 Inogen Rove 6score 29.9 · 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (19)

See all 19

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K011844Merits Health Products Oxygen ConcentratorsMerits Health Products., Inc.200116
K022684Portable Therapeutic Oxygen Concentration System (Ptocs)Essex Cryogenics of Missouri, Inc.20021

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, K011844 (Merits Health Products., Inc., 2001) has gone furthest, with 16 descendants of its own.

How does its category compare?

All CAW devices

CAW Generator, Oxygen, Portable: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CAW

12in 2025

2007: 62008: 112009: 82010: 52011: 62012: 52013: 22014: 62015: 12016: 12017: 12018: 32019: 22020: 52021: 22022: 42023: 82024: 22025: 122026 (partial year): 6
2007high 12 (2025) · low 1 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CAW

178in 2025

2007: 143 days median2008: 90 days median2009: 193 days median2010: 133 days median2011: 174 days median2012: 148 days median2014: 277 days median2018: 203 days median2020: 224 days median2022: 458 days median2023: 261 days median2025: 178 days median2026 (partial year): 260 days median
2007high 458 (2022) · low 90 (2008)2026

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

Recalls per year · CAW

1in 2025

2007: 12008: 32009: 22011: 12013: 22014: 22016: 12017: 12019: 22020: 12022: 22024: 5, 1 Class I2025: 1
2007high 5 (2024) · low 0 (2010)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · CAW

611in 2025

2007: 232008: 252009: 432010: 482011: 1672012: 3952013: 2,3092014: 24,5382015: 18,9732016: 3,1672017: 1072018: 1162019: 1202020: 1252021: 1942022: 3052023: 3572024: 4502025: 611
2007high 24,538 (2014) · low 23 (2007)2025

MAUDE reports naming product code CAW, 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
20076143123
20081190325
20098193243
20105133048
201161741167
201251480395
20132—22,309
20146277224,538
20151—018,973
20161—13,167
20171—1107
201832030116
20192—2120
202052241125
20212—0194
202244582305
202382610357
20242—5 (1)450
2025121781611
202662600—
Cite this page

510(k) Report. “K904087: Mobilaire Iii and V Model Irc 301 and 501 Oxy. Con.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K904087

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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