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FDA 510(k)

IMPLANTING OF POLYACRYLIC FIBERS

K-Number: K770359 · 1977-04-08

Decision Date1977-04-08
Product CodeGBI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IMPLANTING OF POLYACRYLIC FIBERS is the device name listed in this FDA 510(k) record. The listed applicant is Allan V. Marse. It received FDA 510(k) clearance on 1977-04-08 under 510(k) number K770359. The device is classified under product code GBI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANTING OF POLYACRYLIC FIBERS?

IMPLANTING OF POLYACRYLIC FIBERS is a medical device that received FDA 510(k) clearance on 1977-04-08. The listed applicant is Allan V. Marse. The 510(k) number is K770359.

When did IMPLANTING OF POLYACRYLIC FIBERS receive FDA 510(k) clearance?

IMPLANTING OF POLYACRYLIC FIBERS received FDA 510(k) clearance on 1977-04-08, under 510(k) number K770359.

Who is the listed applicant for IMPLANTING OF POLYACRYLIC FIBERS?

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

What is the FDA product code for IMPLANTING OF POLYACRYLIC FIBERS?

The FDA product code for IMPLANTING OF POLYACRYLIC FIBERS is GBI.

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.

Related Devices (Code: GBI)

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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