510(k) Report

510(k) · Cleared

Cleared

Victor Model Ocpr Oxygen Conserving Pressure Regulator

K963247510(k) TraditionalCleared Nov 7, 199680-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

Thermadyne Holings Corp. · NFB Conserver, Oxygen

Cleared on Nov 7, 1996 after an 80-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 9 later devices descend from it.

Decided
Nov 7, 1996
Review
80 days
Class
Class II
Product code
NFB
Recalls
None
Predicates
0

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

Descendants, by year cleared 1999: 1 descendant cleared2002: 1 descendant cleared2003: 1 descendant cleared2006: 2 descendants cleared2007: 1 descendant cleared2005: 1 descendant cleared2009: 1 descendant cleared2025: 1 descendant cleared1995200020052010201520202025
  1. This deviceK963247 Victor Model Ocpr Oxygen Conserving Pressure RegulatorThermadyne Holings Corp. · 1996
  2. Descendant · cites it directly · 8 of its ownK992659 O2N Demand-II, Victor Model Ocpr-IIThermadyne Holings Corp. · 1999
  3. Descendant · 2 generations on · 4 of its ownK031983 Inovo, Inc, Economizer Conserving RegulatorInovo, Inc. · 2003
  4. Descendant · 2 generations on · 3 of its ownK020475 Chad Therapeutics Oxypenumatic Cypress Model 511Chad Therapeutics, Inc. · 2002
  5. Descendant · 3 generations on · 1 of its ownK070740 Chad Therapeutics Bonsai Model 800Chad Therapeutics, Inc. · 2007
  6. Descendant · 3 generations on · 1 of its ownK061785 Cyl-Fil Oxygen SystemResponsive Respiratory, Inc. · 2006

Showing 5 of 9 descendants. See all descendants

Descendants cleared per year

1999: 12002: 12003: 12005: 12006: 22007: 12009: 12025: 1
1999high 2 (2006) · low 0 (2000)2026

Most influential descendants

Showing 5 of 9 · See all
  • K992659O2N Demand-II, Victor Model Ocpr-IIThermadyne Holings Corp. · 1999 · cites it directly8descendants
  • K031983Inovo, Inc, Economizer Conserving RegulatorInovo, Inc. · 2003 · 2 generations on4descendants
  • K020475Chad Therapeutics Oxypenumatic Cypress Model 511Chad Therapeutics, Inc. · 2002 · 2 generations on3descendants
  • K070740Chad Therapeutics Bonsai Model 800Chad Therapeutics, Inc. · 2007 · 3 generations on1descendant
  • K061785Cyl-Fil Oxygen SystemResponsive Respiratory, Inc. · 2006 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K963247Victor Model Ocpr Oxygen Conserving Pressure RegulatorThermadyne Holings Corp.1996—
+1K992659O2N Demand-II, Victor Model Ocpr-IIThermadyne Holings Corp.1999—
+2K031983Inovo, Inc, Economizer Conserving RegulatorInovo, Inc.2003—
+2K020475Chad Therapeutics Oxypenumatic Cypress Model 511Chad Therapeutics, Inc.2002—
+3K070740Chad Therapeutics Bonsai Model 800Chad Therapeutics, Inc.2007—
+3K061785Cyl-Fil Oxygen SystemResponsive Respiratory, Inc.2006—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199910
200210
200310
200510
200620
200710
200910
202510
FIG. 1 — Lineage of K963247, 1996–2025Source: 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 510(k) statement (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?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (9)

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

NumberDeviceApplicantDecidedDescendants
K992659O2N Demand-II, Victor Model Ocpr-IIThermadyne Holings Corp.19998

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, K992659 (Thermadyne Holings Corp., 1999) has gone furthest, with 8 descendants 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 Oxygen Conserving Pressure Regulator (OCPR) is a demand oxygen delivery mode that delivers oxygen only during inspiration while providing oxygen savings equivalent to steady flow. The OCPR extends the useful life of portable oxygen cylinders, increasing oxygen savings and cost savings.

Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K963247: Victor Model Ocpr Oxygen Conserving Pressure Regulator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K963247

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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