510(k) Report

510(k) · Cleared

Cleared

Pad, Examining Table

K801936510(k) TraditionalCleared Aug 27, 198015-day reviewClass I21 CFR 880.6140

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

Volunteer Blind Industries, Inc. · KMN Chair And Table, Medical

Cleared on Aug 27, 1980 after a 15-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Aug 27, 1980
Review
15 days
Class
Class I
Product code
KMN
Recalls
None
Predicates
0

FDA has not posted a summary or statement for it, so its predicates are not known.

FIG. 1 — Lineage of K801936Source: FDA 510(k) database · 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 KMN? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

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  • Recall history across each candidate’s familyin the report
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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?

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.

How does its category compare?

All KMN devices

KMN Chair And Table, Medical: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KMN

FDA has decided no KMN device since 2007.

Median 510(k) review, days · KMN

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

Recalls per year · KMN

No recall names KMN since 2007.

Adverse event reports per year · KMN

1in 2025

2007: 32009: 62010: 52011: 72012: 112013: 62014: 82015: 222016: 112017: 22018: 72019: 22020: 32022: 22023: 102024: 12025: 1
2007high 22 (2015) · low 0 (2008)2025

MAUDE reports naming product code KMN, 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
20070—03
20080—00
20090—06
20100—05
20110—07
20120—011
20130—06
20140—08
20150—022
20160—011
20170—02
20180—07
20190—02
20200—03
20210—00
20220—02
20230—010
20240—01
20250—01
20260—0—

More from Volunteer Blind Industries, Inc.

2 FDA decisions under this applicant name. See the company

  • K801935Pad, Hospital StretcherVolunteer Blind Industries, Inc. · 1980

Recent decisions in KMN

The KMN category page

  • K894788Dmi Series 90 Examination TableM.D. Intl., Inc. · 1989
  • K761110Bed TrayFred Sammons, Inc. · 1976

https://510kreport.com/device/K801936 · printed Nov 4, 2026

Cite this page

510(k) Report. “K801936: Pad, Examining Table.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K801936

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Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026