510(k) Report

510(k) · Cleared

Cleared

Captain's Chair Accessory to Amsco Surgical Tables

K935356510(k) TraditionalCleared Mar 23, 1994139-day reviewClass I21 CFR 878.4960

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

Amsco American Sterilizer Co. · FWW Table, Operating-Room, Pneumatic

Cleared on Mar 23, 1994 after a 139-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Decided
Mar 23, 1994
Review
139 days
Class
Class I
Product code
FWW
Recalls
None
Predicates
0

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

FIG. 1 — Lineage of K935356Source: 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 FWW? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, 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 FWW devices

FWW Table, Operating-Room, Pneumatic: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FWW

FDA has decided no FWW device since 2007.

Median 510(k) review, days · FWW

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

Recalls per year · FWW

No recall names FWW since 2007.

Adverse event reports per year · FWW

1in 2025

2007: 12018: 22019: 52020: 22021: 12022: 62023: 12024: 32025: 1
2007high 6 (2022) · low 0 (2008)2025

MAUDE reports naming product code FWW, 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—01
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—02
20190—05
20200—02
20210—01
20220—06
20230—01
20240—03
20250—01
20260—0—
Cite this page

510(k) Report. “K935356: Captain's Chair Accessory to Amsco Surgical Tables.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K935356

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