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FDA 510(k)

AMSCO SURGICAL TABLE

K-Number: K971307 · 1997-06-27

ApplicantSTERIS Corporation
Decision Date1997-06-27
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AMSCO SURGICAL TABLE is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 1997-06-27 under 510(k) number K971307. The device is classified under product code FQO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMSCO SURGICAL TABLE?

AMSCO SURGICAL TABLE is a medical device that received FDA 510(k) clearance on 1997-06-27. The listed applicant is STERIS Corporation. The 510(k) number is K971307.

When did AMSCO SURGICAL TABLE receive FDA 510(k) clearance?

AMSCO SURGICAL TABLE received FDA 510(k) clearance on 1997-06-27, under 510(k) number K971307.

Who is the listed applicant for AMSCO SURGICAL TABLE?

The FDA 510(k) record lists STERIS Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMSCO SURGICAL TABLE?

The FDA product code for AMSCO SURGICAL TABLE is FQO.

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Related Devices (Code: FQO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K240598Maestro System (REF100)Moon SurgicalK221410Maestro PlatformMoon SurgicalK090136STERIS CMAX XLT SURGICAL TABLESTERIS CorporationK972810OPT80 THE TRANSPORTABLE (OPT80)O.P.T. USA, Inc.K971988ALLEN, ULTRA AND SMART SOCKETSAllen Medical Systems, Inc.K963506TENET RADIOLUCENT HAND TABLETenet Medical Engineering

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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