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FDA 510(k)

OPERATING TABLE ACCESSORY CLAMP

K-Number: K810282 · 1981-02-26

ApplicantMinnesota Scientific, Inc.
Decision Date1981-02-26
Product CodeGBJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OPERATING TABLE ACCESSORY CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Minnesota Scientific, Inc.. It received FDA 510(k) clearance on 1981-02-26 under 510(k) number K810282. The device is classified under product code GBJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPERATING TABLE ACCESSORY CLAMP?

OPERATING TABLE ACCESSORY CLAMP is a medical device that received FDA 510(k) clearance on 1981-02-26. The listed applicant is Minnesota Scientific, Inc.. The 510(k) number is K810282.

When did OPERATING TABLE ACCESSORY CLAMP receive FDA 510(k) clearance?

OPERATING TABLE ACCESSORY CLAMP received FDA 510(k) clearance on 1981-02-26, under 510(k) number K810282.

Who is the listed applicant for OPERATING TABLE ACCESSORY CLAMP?

The FDA 510(k) record lists Minnesota Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPERATING TABLE ACCESSORY CLAMP?

The FDA product code for OPERATING TABLE ACCESSORY CLAMP is GBJ.

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Other records listing Minnesota Scientific, Inc. 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.

K872919OMNI-TRACT CORRAL RETRACTORK853948MINNESOTA SCIENTIFIC, INC. OMNI-BEAMK853947OMNI-TRACT CHEST WALL & LUNA RETRACTORK842762OMNI-TRACT SURGICAL RETRACTOR SYS

Related Devices (Code: GBJ)

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.

K934970DUETTrulife , Ltd.K790946GORDON IVS INTRAVENOUS STABILIZERWhitman Medical Corp.K790186PROTECTIVSTABILIZERJelco Laboratories

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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