BANDAGE, RAPIDO-LASTIC COTTON/NYLON
K-Number: K760142 · 1976-07-19
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Device Summary
Frequently Asked Questions
What is the BANDAGE, RAPIDO-LASTIC COTTON/NYLON?
BANDAGE, RAPIDO-LASTIC COTTON/NYLON 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 K760142.
When did BANDAGE, RAPIDO-LASTIC COTTON/NYLON receive FDA 510(k) clearance?
BANDAGE, RAPIDO-LASTIC COTTON/NYLON received FDA 510(k) clearance on 1976-07-19, under 510(k) number K760142.
Who is the listed applicant for BANDAGE, RAPIDO-LASTIC COTTON/NYLON?
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, RAPIDO-LASTIC COTTON/NYLON?
The FDA product code for BANDAGE, RAPIDO-LASTIC COTTON/NYLON 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.
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