510(k) Report

510(k) · Cleared

Cleared

Compressor Filter, Models AG1038831, HCF100,BF900,BF910,BF950, LL201, LL202, LL205, Bacteria Filter

K091363510(k) TraditionalCleared Feb 4, 2010272-day reviewClass II21 CFR 868.5260

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

Ag Industries · CAH Filter, Bacterial, Breathing-Circuit

Cleared on Feb 4, 2010 as substantially equivalent to K061426 (Porous Media Corp., 2006) after a 272-day review. Its family tree reaches back 7 generations to 1994. 1 later device descends from it.

Decided
Feb 4, 2010
Review
272 days
Class
Class II
Product code
CAH
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K933081 (1994). 17 ancestors in all, the oldest K792097 (1979). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 1 other ancestor2002: 1 other ancestor1999: 1 other ancestor1998: 1 other ancestor1995: 1 other ancestor1996: 1 other ancestor2001: 1 other ancestor1994: 1 other ancestor1979: 1 other ancestor1985: 1 other ancestor2014: 1 descendant clearedK933081 · Oxlife Oxygen Concentrator · Oxlife, Inc. · 1994K955549 · Oxlife Oxygen Concentrators · Oxlife, Inc. · 1996K963042 · Innosan Travelair S Portable Oxygen Concentrator, Code NO. M407001853 · Sim Italia S.R.L. · 1996K013931 · Omni Oxygen System, Model 1000 · Sequal Technologies, Inc. · 2002 · recalled×2: 2 generations cleared close together, K042262 (2004), K043006 (2005) K061426 · Oxygen Concentrator Filters, Models DBF32, DBF24, DBF27, DBF25, DFC06 and DDF47 · Porous Media Corp. · 200619801990200020102020
  1. Root · 7 generations backK933081 Oxlife Oxygen ConcentratorOxlife, Inc. · 1994
  2. 6 generations backK955549 Oxlife Oxygen ConcentratorsOxlife, Inc. · 1996
  3. 5 generations backK963042 Innosan Travelair S Portable Oxygen Concentrator, Code NO. M407001853Sim Italia S.R.L. · 1996
  4. 4 generations backK013931 Omni Oxygen System, Model 1000Sequal Technologies, Inc. · 2002 · Recalled
  5. 3 generations backK042262 Integra Oxygen Concentrator, Model 6323A-OM-10Sequal Technologies, Inc. · 2004
  6. 2 generations backK043006 Millennium M10 Oxygen Concentrator, Model M10600; with Opi, Model…Respironics, Inc. · 2005
  7. 1 generation backK061426 Oxygen Concentrator Filters, Models DBF32, DBF24, DBF27, DBF25…Porous Media Corp. · 2006
  8. This deviceK091363 Compressor Filter, Models AG1038831, HCF100,BF900,BF910,BF950…Ag Industries · 2010
  9. Descendant · cites it directly · 0 of its ownK131626 Exceleron Bacterial FiltersExceleron Medical · 2014

Most influential descendants

Showing 1 of 1 · See all
  • K131626Exceleron Bacterial FiltersExceleron Medical · 2014 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K933081Oxlife Oxygen ConcentratorOxlife, Inc.1994—
−6K955549Oxlife Oxygen ConcentratorsOxlife, Inc.1996—
−5K963042Innosan Travelair S Portable Oxygen Concentrator, Code NO. M407001853Sim Italia S.R.L.1996—
−4K013931Omni Oxygen System, Model 1000Sequal Technologies, Inc.20021
−3K042262Integra Oxygen Concentrator, Model 6323A-OM-10Sequal Technologies, Inc.2004—
−2K043006Millennium M10 Oxygen Concentrator, Model M10600; with Opi, Model M10605Respironics, Inc.2005—
−1K061426Oxygen Concentrator Filters, Models DBF32, DBF24, DBF27, DBF25, DFC06 and DDF47Porous Media Corp.2006—
0 (this device)K091363Compressor Filter, Models AG1038831, HCF100,BF900,BF910,BF950, LL201, LL202…Ag Industries2010—
+1K131626Exceleron Bacterial FiltersExceleron Medical2014—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198510
199410
199510
199610
199810
199910
200110
200210
200510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
FIG. 1 — Lineage of K091363, 1994–2014Source: 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), 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 CAH? 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 CAH device

  1. #1 K251583 Ambu® Virobac II® Exhalation Filterscore 11.6 · 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
*K061426Oxygen Concentrator Filters, Models DBF32, DBF24, DBF27, DBF25, DFC06 and DDF47
Summary page 1
…3. Predicate Device Information: Comparison to Predicate Devices: The above devices are compared to similar devices marketed by Porous Media which were cleared under K061426. The features of each are exhibited in the following tables. 9…
Porous Media Corp.2006—

Also cleared against K061426: 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
K131626Exceleron Bacterial FiltersExceleron Medical20140

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 6 companies; a new generation was cleared every 1.4 years on median.
  • 3 of the 17 ancestors have a recall of any class.
  • Of its descendants, K131626 (Exceleron Medical, 2014) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K061426.

How does its category compare?

All CAH devices

CAH Filter, Bacterial, Breathing-Circuit: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · CAH

2in 2024

2007: 22008: 12009: 42010: 52011: 32012: 32013: 12014: 42015: 22017: 12019: 22020: 22021: 22022: 32023: 32024: 22026 (partial year): 2
2007high 5 (2010) · low 0 (2016)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CAH

237in 2023

2009: 111 days median2010: 216 days median2011: 281 days median2012: 212 days median2014: 250 days median2022: 204 days median2023: 237 days median
2007high 281 (2011) · low 111 (2009)2026

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

Recalls per year · CAH

1in 2025

2010: 22013: 12014: 12017: 12022: 6, 6 Class I2025: 1, 1 Class I
2007high 6 (2022) · low 0 (2007)2026

Class I (7 since 2007) Class II/III not classified

Adverse event reports per year · CAH

77in 2025

2007: 322008: 272009: 182010: 402011: 92012: 162013: 472014: 982015: 512016: 342017: 292018: 332019: 302020: 332021: 562022: 672023: 402024: 512025: 77
2007high 98 (2014) · low 9 (2011)2025

MAUDE reports naming product code CAH, 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—032
20081—027
20094111018
20105216240
2011328109
20123212016
20131—147
20144250198
20152—051
20160—034
20171—129
20180—033
20192—030
20202—033
20212—056
202232046 (6)67
20233237040
20242—051
20250—1 (1)77
20262—0—

What is it indicated for?

AG Industries filters are replacement filters intended for use in oxygen concentrator machines to help remove contaminants, including air borne bacteria and other particulate debris from an air stream. When used with oxygen concentrator machines, the replacement filters may be used in the home, nursing home, hospital, patient care facility, etc.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K091363: Compressor Filter, Models AG1038831, HCF100,BF900,BF910,BF950, LL201, LL202, LL205, Bacteria Filter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K091363

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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