LIQUID BANDAGE
K-Number: K120059 · 2012-05-17
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Device Summary
Frequently Asked Questions
What is the LIQUID BANDAGE?
LIQUID BANDAGE is a medical device that received FDA 510(k) clearance on 2012-05-17. The listed applicant is Chesson Laboratory Associates, Inc.. The 510(k) number is K120059.
When did LIQUID BANDAGE receive FDA 510(k) clearance?
LIQUID BANDAGE received FDA 510(k) clearance on 2012-05-17, under 510(k) number K120059.
Who is the listed applicant for LIQUID BANDAGE?
The FDA 510(k) record lists Chesson Laboratory Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUID BANDAGE?
The FDA product code for LIQUID 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 Chesson Laboratory Associates, Inc. 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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