FALKON STRETCH
K-Number: K854432 · 1985-11-22
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement