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FDA 510(k)

GENERAL SURGICAL TABLE AND ACCESSORIES

K-Number: K882660 · 1988-07-25

Decision Date1988-07-25
Product CodeFQO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GENERAL SURGICAL TABLE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is American Sterilizer Co.. It received FDA 510(k) clearance on 1988-07-25 under 510(k) number K882660. 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 GENERAL SURGICAL TABLE AND ACCESSORIES?

GENERAL SURGICAL TABLE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1988-07-25. The listed applicant is American Sterilizer Co.. The 510(k) number is K882660.

When did GENERAL SURGICAL TABLE AND ACCESSORIES receive FDA 510(k) clearance?

GENERAL SURGICAL TABLE AND ACCESSORIES received FDA 510(k) clearance on 1988-07-25, under 510(k) number K882660.

Who is the listed applicant for GENERAL SURGICAL TABLE AND ACCESSORIES?

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

What is the FDA product code for GENERAL SURGICAL TABLE AND ACCESSORIES?

The FDA product code for GENERAL SURGICAL TABLE AND ACCESSORIES is FQO.

Related Clinical Trials

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.

Other records listing American Sterilizer Co. as applicant

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.

View all 36 devices →

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.

Official Source

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

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