510(k) Report

510(k) · Cleared

Cleared

Dispos. Hyperbaric Oxygen Cush/Traum

K831825510(k) TraditionalCleared Oct 27, 1983142-day reviewClass II21 CFR 878.5650

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

Hospitak, Inc. · KPJ Chamber, Oxygen, Topical, Extremity

Cleared on Oct 27, 1983 after a 142-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 11 later devices descend from it.

Decided
Oct 27, 1983
Review
142 days
Class
Class II
Product code
KPJ
Recalls
None
Predicates
0

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

Descendants, by year cleared 1997: 1 descendant cleared2003: 1 descendant cleared2008: 1 descendant cleared2002: 1 descendant cleared2005: 1 descendant cleared2012: 2 descendants cleared2009: 1 descendant cleared2023: 1 descendant cleared2019: 1 descendant cleared2025: 1 descendant cleared19801990200020102020
  1. This deviceK831825 Dispos. Hyperbaric Oxygen Cush/TraumHospitak, Inc. · 1983
  2. Descendant · cites it directly · 10 of its ownK971507 O2 BOOTGwr Medical, Llp · 1997
  3. Descendant · 2 generations on · 4 of its ownK023456 Oxybox SystemOxyfast Corporation · 2003 · Recalled
  4. Descendant · 2 generations on · 4 of its ownK022028 VX-400 Topical Hyperbaric Oxygen ChamberVascular One, Inc. · 2002
  5. Descendant · 2 generations on · 2 of its ownK080966 Hyper-Box Topical Wound Oxygen SystemAoti, Ltd. · 2008
  6. Descendant · 3 generations on · 1 of its ownK212121 VHT-200 Wound Treatment SystemVaporox, Inc. · 2023

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

1997: 12002: 12003: 12005: 12008: 12009: 12012: 22019: 12023: 12025: 1
1997high 2 (2012) · low 0 (1998)2026

Most influential descendants

Showing 5 of 11 · See all
  • K971507O2 BOOTGwr Medical, Llp · 1997 · cites it directly10descendants
  • K023456Oxybox SystemOxyfast Corporation · 2003 · 2 generations on4descendants
  • K022028VX-400 Topical Hyperbaric Oxygen ChamberVascular One, Inc. · 2002 · 2 generations on4descendants
  • K080966Hyper-Box Topical Wound Oxygen SystemAoti, Ltd. · 2008 · 2 generations on2descendants
  • K212121VHT-200 Wound Treatment SystemVaporox, Inc. · 2023 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K831825Dispos. Hyperbaric Oxygen Cush/TraumHospitak, Inc.1983—
+1K971507O2 BOOTGwr Medical, Llp1997—
+2K023456Oxybox SystemOxyfast Corporation20032
+2K022028VX-400 Topical Hyperbaric Oxygen ChamberVascular One, Inc.2002—
+2K080966Hyper-Box Topical Wound Oxygen SystemAoti, Ltd.2008—
+3K212121VHT-200 Wound Treatment SystemVaporox, Inc.2023—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199710
200210
200310
200510
200810
200910
201220
201910
202310
202510
FIG. 1 — Lineage of K831825, 1983–2025Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KPJ? 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 KPJ device

  1. #1 K250188 Wound Treatment System (VHT-200)score 10.2 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
Get a 510(k) Report

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? (11)

See all 11

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

NumberDeviceApplicantDecidedDescendants
K971507O2 BOOTGwr Medical, Llp199710

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, K971507 (Gwr Medical, Llp, 1997) has gone furthest, with 10 descendants of its own.

How does its category compare?

All KPJ devices

KPJ Chamber, Oxygen, Topical, Extremity: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KPJ

1in 2025

2008: 12009: 12012: 22019: 12023: 12025: 1
2007high 2 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KPJ

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

Recalls per year · KPJ

1in 2012

2012: 1
2007high 1 (2012) · low 0 (2007)2026

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

Adverse event reports per year · KPJ

No MAUDE report names KPJ since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20081—00
20091—00
20100—00
20110—00
20122—10
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20191—00
20200—00
20210—00
20220—00
20231—00
20240—00
20251—00
20260—0—
Cite this page

510(k) Report. “K831825: Dispos. Hyperbaric Oxygen Cush/Traum.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K831825

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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