510(k) Report

510(k) · Cleared

Cleared

Pulsed Oxygen Conserving Device - Every Breath, Pocdeb, Reacteb

K023420510(k) SpecialCleared Oct 25, 200214-day reviewClass II21 CFR 868.5905

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

Medical Electronic Devices, Inc. · NFB Conserver, Oxygen

Cleared on Oct 25, 2002 as substantially equivalent to K983459 (Medical Electronic Devices, Inc., 1998) after a 14-day review. Its family tree reaches back 2 generations to 1985. 2 later devices descend from it.

Decided
Oct 25, 2002
Review
14 days
Class
Class II
Product code
NFB
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K852650 (1985). 4 ancestors in all. 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1996: 1 other ancestor1989: 1 other ancestor2004: 1 descendant cleared2005: 1 descendant clearedK852650 · Oxymatictm Electronic Oxgyen Conserver · Chad Therapeutics, Inc. · 1985K983459 · Pulsed Oxygen Conserving Device, Pocd · Medical Electronic Devices, Inc. · 19981990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 2 other ancestors 1 generation forward: 1 descendant2 generations forward: 1 descendant K983459 · Pulsed Oxygen Conserving Device, Pocd · Medical Electronic Devices, Inc. · 1998K852650 · Oxymatictm Electronic Oxgyen Conserver · Chad Therapeutics, Inc. · 19850
  1. Root · 2 generations backK852650 Oxymatictm Electronic Oxgyen ConserverChad Therapeutics, Inc. · 1985
  2. 1 generation backK983459 Pulsed Oxygen Conserving Device, PocdMedical Electronic Devices, Inc. · 1998
  3. This deviceK023420 Pulsed Oxygen Conserving Device - Every Breath, Pocdeb, ReactebMedical Electronic Devices, Inc. · 2002
  4. Descendant · cites it directly · 1 of its ownK033197 Inogen Satellite ConserverMedical Electronic Devices, Inc. · 2004
  5. Descendant · 2 generations on · 0 of its ownK052563 Inogen Satellite Conserver, Model SC-100Medical Electronic Devices, Inc. · 2005

Most influential descendants

Showing 2 of 2 · See all
  • K033197Inogen Satellite ConserverMedical Electronic Devices, Inc. · 2004 · cites it directly1descendant
  • K052563Inogen Satellite Conserver, Model SC-100Medical Electronic Devices, Inc. · 2005 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K852650Oxymatictm Electronic Oxgyen ConserverChad Therapeutics, Inc.1985—
−1K983459Pulsed Oxygen Conserving Device, PocdMedical Electronic Devices, Inc.1998—
0 (this device)K023420Pulsed Oxygen Conserving Device - Every Breath, Pocdeb, ReactebMedical Electronic Devices, Inc.2002—
+1K033197Inogen Satellite ConserverMedical Electronic Devices, Inc.2004—
+2K052563Inogen Satellite Conserver, Model SC-100Medical Electronic Devices, Inc.2005—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
199610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
200510
FIG. 1 — Lineage of K023420, 1985–2005Source: 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 NFB? 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 NFB device

  1. #1 K250322 Respond OC Conserving Regulator (130-0800)score 10.6 · 4 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? (2)

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
*K983459Pulsed Oxygen Conserving Device, Pocd
Summary page 1
…Predicate Device Equivalence: Substantial equivalence is claimed to the Medical Electronic Devices Corporation unmodified POCD, cleared for commercial distribution per K983459 and the CHAD Therapeutics OXYMATIC Model 311. Device Description: The Medical Electronic Devices Corp. POCDEBintended to be us…
Medical Electronic Devices, Inc.1998—
*—CHAD Therapeutics OXYMATIC Model 311
Named without a submission number
—

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K033197Inogen Satellite ConserverMedical Electronic Devices, Inc.20041

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 2 companies; a new generation was cleared every 13.3 years on median.
  • None of the 4 ancestors has a recall.
  • Of its descendants, K033197 (Medical Electronic Devices, Inc., 2004) has gone furthest, with 1 descendant of its own.

How does its category compare?

All NFB devices

NFB Conserver, Oxygen: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · NFB

1in 2025

2007: 12009: 12010: 12011: 12013: 12016: 12020: 12022: 22025: 1
2007high 2 (2022) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NFB

Too few NFB 510(k)s in any year since 2007 to give a median.

Recalls per year · NFB

3in 2007

2007: 3
2007high 3 (2007) · low 0 (2008)2026

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

Adverse event reports per year · NFB

8in 2025

2007: 32011: 12012: 32013: 52014: 22015: 42017: 92020: 32021: 22022: 12023: 42024: 12025: 8
2007high 9 (2017) · low 0 (2008)2025

MAUDE reports naming product code NFB, 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
20071—33
20080—00
20091—00
20101—00
20111—01
20120—03
20131—05
20140—02
20150—04
20161—00
20170—09
20180—00
20190—00
20201—03
20210—02
20222—01
20230—04
20240—01
20251—08
20260—0—

What is it indicated for?

The modified Medical Electronic Devices Corp. POCD Pulsed Oxygen Conserving Device is intended for use in the same manner as the unmodified device, i.e., to conserve oxygen for patients prescribed 1 to 4 liters per minute of supplemental oxygen and use nasal cannulas and USP bottled oxygen.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K023420: Pulsed Oxygen Conserving Device - Every Breath, Pocdeb, Reacteb.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K023420

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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