BANDAGE, GAUZE, SIX-PLY, VARIOUS SIZES
K-Number: K863714 · 1986-10-14
Advertisement
Device Summary
Frequently Asked Questions
What is the BANDAGE, GAUZE, SIX-PLY, VARIOUS SIZES?
BANDAGE, GAUZE, SIX-PLY, VARIOUS SIZES is a medical device that received FDA 510(k) clearance on 1986-10-14. The listed applicant is Fraass Survival Systems, Inc.. The 510(k) number is K863714.
When did BANDAGE, GAUZE, SIX-PLY, VARIOUS SIZES receive FDA 510(k) clearance?
BANDAGE, GAUZE, SIX-PLY, VARIOUS SIZES received FDA 510(k) clearance on 1986-10-14, under 510(k) number K863714.
Who is the listed applicant for BANDAGE, GAUZE, SIX-PLY, VARIOUS SIZES?
The FDA 510(k) record lists Fraass Survival Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BANDAGE, GAUZE, SIX-PLY, VARIOUS SIZES?
The FDA product code for BANDAGE, GAUZE, SIX-PLY, VARIOUS SIZES 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 Fraass Survival Systems, 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