BANDAGE, WRINKY-LASTIC ELASTIC GAUZE
K-Number: K760140 · 1976-07-19
Advertisement
Device Summary
Frequently Asked Questions
What is the BANDAGE, WRINKY-LASTIC ELASTIC GAUZE?
BANDAGE, WRINKY-LASTIC ELASTIC GAUZE is a medical device that received FDA 510(k) clearance on 1976-07-19. The listed applicant is Conco Medical Co.. The 510(k) number is K760140.
When did BANDAGE, WRINKY-LASTIC ELASTIC GAUZE receive FDA 510(k) clearance?
BANDAGE, WRINKY-LASTIC ELASTIC GAUZE received FDA 510(k) clearance on 1976-07-19, under 510(k) number K760140.
Who is the listed applicant for BANDAGE, WRINKY-LASTIC ELASTIC GAUZE?
The FDA 510(k) record lists Conco Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BANDAGE, WRINKY-LASTIC ELASTIC GAUZE?
The FDA product code for BANDAGE, WRINKY-LASTIC ELASTIC GAUZE is FQM.
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 Conco Medical Co. 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: FQM)
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