510(k) Report

510(k) · Cleared

Cleared

Pogs, Model 65/130

K092636510(k) TraditionalCleared Jan 7, 2010133-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

On Site Gas Systems, Inc. · CAW Generator, Oxygen, Portable

Cleared on Jan 7, 2010 as substantially equivalent to K063454 (On Site Gas Systems, Inc., 2007) after a 133-day review. Its family tree reaches back 8 generations to 1994.

Decided
Jan 7, 2010
Review
133 days
Class
Class II
Product code
CAW
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K933081 (1994). 12 ancestors in all, the oldest K904087 (1990). No later device cites it as a predicate yet.

  1. Root · 8 generations backK933081 Oxlife Oxygen ConcentratorOxlife, Inc. · 1994
  2. 7 generations backK955549 Oxlife Oxygen ConcentratorsOxlife, Inc. · 1996
  3. 6 generations backK011844 Merits Health Products Oxygen ConcentratorsMerits Health Products., Inc. · 2001
  4. 5 generations backK014078 ON Site Gas Systems Portable Oxygen Generator SystemOn Site Gas Systems, Inc. · 2002
  5. 4 generations backK020362 P.O.G.S. 3.3 Portable Oxygen Generator SystemOn Site Gas Systems, Inc. · 2002
  6. 3 generations backK030920 POGS 33On Site Gas Systems, Inc. · 2004
  7. 2 generations backK041664 Portable Oxygen Generation System: Pogs 33COn Site Gas Systems, Inc. · 2004
  8. 1 generation backK063454 Pogs, Model 33COn Site Gas Systems, Inc. · 2007
  9. This deviceK092636 Pogs, Model 65/130On Site Gas Systems, Inc. · 2010
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K933081Oxlife Oxygen ConcentratorOxlife, Inc.1994—
−7K955549Oxlife Oxygen ConcentratorsOxlife, Inc.1996—
−6K011844Merits Health Products Oxygen ConcentratorsMerits Health Products., Inc.2001—
−5K014078ON Site Gas Systems Portable Oxygen Generator SystemOn Site Gas Systems, Inc.2002—
−4K020362P.O.G.S. 3.3 Portable Oxygen Generator SystemOn Site Gas Systems, Inc.2002—
−3K030920POGS 33On Site Gas Systems, Inc.2004—
−2K041664Portable Oxygen Generation System: Pogs 33COn Site Gas Systems, Inc.2004—
−1K063454Pogs, Model 33COn Site Gas Systems, Inc.2007—
0 (this device)K092636Pogs, Model 65/130On Site Gas Systems, Inc.2010—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199720
200210
FIG. 1 — Lineage of K092636, 1994–2010Source: 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 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? (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
*K063454Pogs, Model 33C
Summary page 1
…Product Code: CAW Classification Panel: Anesthesiology Regulation Number: 21 CFR 868.5440 Predicate Devices: P0GS 33C, 5 10(k) K063454, On-Site Gas Systej.. n.' Description of Device: ortbleOxygen Generation Sy-ste-m-6-5/130o(PG The person…
On Site Gas Systems, Inc.2007—

Also cleared against K063454: 1 other device →

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 16 years and passes through 3 companies; a new generation was cleared every 2.1 years on median.
  • None of the 12 ancestors has a recall.
  • 1 other device also cites its predicate K063454.

How does its category compare?

All CAW devices

CAW Generator, Oxygen, Portable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

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—

What is it indicated for?

The FOGS 65/130 is intended to generate and deliver USP 93% supplemental oxygen. This device is intended to be used only by trained personnel in disaster relief and emergehcy preparedness situations, military settings or where bottled oxygen is not readily available

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K092636: Pogs, Model 65/130.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K092636

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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