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FDA 510(k)

FELDSTEIN BLEPHAROPLASTY CLIP RECTANGU

K-Number: K760848 · 1976-11-02

Decision Date1976-11-02
Product CodeHNC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FELDSTEIN BLEPHAROPLASTY CLIP RECTANGU 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 K760848. The device is classified under product code HNC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FELDSTEIN BLEPHAROPLASTY CLIP RECTANGU?

FELDSTEIN BLEPHAROPLASTY CLIP RECTANGU 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 K760848.

When did FELDSTEIN BLEPHAROPLASTY CLIP RECTANGU receive FDA 510(k) clearance?

FELDSTEIN BLEPHAROPLASTY CLIP RECTANGU received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760848.

Who is the listed applicant for FELDSTEIN BLEPHAROPLASTY CLIP RECTANGU?

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 FELDSTEIN BLEPHAROPLASTY CLIP RECTANGU?

The FDA product code for FELDSTEIN BLEPHAROPLASTY CLIP RECTANGU is HNC.

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 V. Mueller O.V. Baxter Healthcare Corp. 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 41 devices →

Related Devices (Code: HNC)

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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