LIQUIDERM LIQUID ADHESIVE BANDAGE
K-Number: K002338 · 2001-01-29
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Device Summary
Frequently Asked Questions
What is the LIQUIDERM LIQUID ADHESIVE BANDAGE?
LIQUIDERM LIQUID ADHESIVE BANDAGE is a medical device that received FDA 510(k) clearance on 2001-01-29. The listed applicant is Closure Medical Corp.. The 510(k) number is K002338.
When did LIQUIDERM LIQUID ADHESIVE BANDAGE receive FDA 510(k) clearance?
LIQUIDERM LIQUID ADHESIVE BANDAGE received FDA 510(k) clearance on 2001-01-29, under 510(k) number K002338.
Who is the listed applicant for LIQUIDERM LIQUID ADHESIVE BANDAGE?
The FDA 510(k) record lists Closure Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUIDERM LIQUID ADHESIVE BANDAGE?
The FDA product code for LIQUIDERM LIQUID ADHESIVE BANDAGE is KMF.
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 Closure Medical Corp. 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: KMF)
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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