STRIP, CLOSED CELL FOAM, BK-7171
K-Number: K760299 · 1976-09-08
Advertisement
Device Summary
Frequently Asked Questions
What is the STRIP, CLOSED CELL FOAM, BK-7171?
STRIP, CLOSED CELL FOAM, BK-7171 is a medical device that received FDA 510(k) clearance on 1976-09-08. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K760299.
When did STRIP, CLOSED CELL FOAM, BK-7171 receive FDA 510(k) clearance?
STRIP, CLOSED CELL FOAM, BK-7171 received FDA 510(k) clearance on 1976-09-08, under 510(k) number K760299.
Who is the listed applicant for STRIP, CLOSED CELL FOAM, BK-7171?
The FDA 510(k) record lists Fred Sammons, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STRIP, CLOSED CELL FOAM, BK-7171?
The FDA product code for STRIP, CLOSED CELL FOAM, BK-7171 is ILH.
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 Fred Sammons, 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: ILH)
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