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FDA 510(k)

CIRCULON(TM) ADHESIVE COMPRESSION BANDAGE

K-Number: K912518 · 1991-09-04

Decision Date1991-09-04
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CIRCULON(TM) ADHESIVE COMPRESSION BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. It received FDA 510(k) clearance on 1991-09-04 under 510(k) number K912518. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 81 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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