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FDA 510(k)

FALKON STRETCH

K-Number: K854432 · 1985-11-22

Decision Date1985-11-22
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

FALKON STRETCH is the device name listed in this FDA 510(k) record. The listed applicant is G.B.F. Industries, Inc.. It received FDA 510(k) clearance on 1985-11-22 under 510(k) number K854432. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FALKON STRETCH?

FALKON STRETCH is a medical device that received FDA 510(k) clearance on 1985-11-22. The listed applicant is G.B.F. Industries, Inc.. The 510(k) number is K854432.

When did FALKON STRETCH receive FDA 510(k) clearance?

FALKON STRETCH received FDA 510(k) clearance on 1985-11-22, under 510(k) number K854432.

Who is the listed applicant for FALKON STRETCH?

The FDA 510(k) record lists G.B.F. Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FALKON STRETCH?

The FDA product code for FALKON STRETCH is EFQ.

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 G.B.F. Industries, 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.

Related Devices (Code: EFQ)

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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