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FDA 510(k)

INSTRUMENT RACK FOR DAWSON-YUHL INSTR.

K-Number: K760579 · 1976-11-02

ApplicantV. Mueller O.V. Baxter Healthcare Corp.
Decision Date1976-11-02
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INSTRUMENT RACK FOR DAWSON-YUHL INSTR. is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1976-11-02 under 510(k) number K760579. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT RACK FOR DAWSON-YUHL INSTR.?

INSTRUMENT RACK FOR DAWSON-YUHL INSTR. is a medical device that received FDA 510(k) clearance on 1976-11-02. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760579.

When did INSTRUMENT RACK FOR DAWSON-YUHL INSTR. receive FDA 510(k) clearance?

INSTRUMENT RACK FOR DAWSON-YUHL INSTR. received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760579.

Who is the listed applicant for INSTRUMENT RACK FOR DAWSON-YUHL INSTR.?

The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTRUMENT RACK FOR DAWSON-YUHL INSTR.?

The FDA product code for INSTRUMENT RACK FOR DAWSON-YUHL INSTR. is FSM.

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Other records listing V. Mueller O.V. Baxter Healthcare Corp. as applicant

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Related Devices (Code: FSM)

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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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