CIRCULON(TM) ADHESIVE COMPRESSION BANDAGE
K-Number: K912518 · 1991-09-04
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Device Summary
Frequently Asked Questions
What is the CIRCULON(TM) ADHESIVE COMPRESSION BANDAGE?
CIRCULON(TM) ADHESIVE COMPRESSION BANDAGE is a medical device that received FDA 510(k) clearance on 1991-09-04. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K912518.
When did CIRCULON(TM) ADHESIVE COMPRESSION BANDAGE receive FDA 510(k) clearance?
CIRCULON(TM) ADHESIVE COMPRESSION BANDAGE received FDA 510(k) clearance on 1991-09-04, under 510(k) number K912518.
Who is the listed applicant for CIRCULON(TM) ADHESIVE COMPRESSION BANDAGE?
The FDA 510(k) record lists Convatec, A Division of E.R. Squibb & Sons as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CIRCULON(TM) ADHESIVE COMPRESSION BANDAGE?
The FDA product code for CIRCULON(TM) ADHESIVE COMPRESSION BANDAGE is KGX.
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 Convatec, A Division of E.R. Squibb & Sons 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: KGX)
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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