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FDA 510(k)

CHESSON LABS LIQUID BANDAGE

K-Number: K083913 · 2009-07-31

ApplicantChesson Laboratory Associates, Inc.
Decision Date2009-07-31
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHESSON LABS LIQUID BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Chesson Laboratory Associates, Inc.. It received FDA 510(k) clearance on 2009-07-31 under 510(k) number K083913. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHESSON LABS LIQUID BANDAGE?

CHESSON LABS LIQUID BANDAGE is a medical device that received FDA 510(k) clearance on 2009-07-31. The listed applicant is Chesson Laboratory Associates, Inc.. The 510(k) number is K083913.

When did CHESSON LABS LIQUID BANDAGE receive FDA 510(k) clearance?

CHESSON LABS LIQUID BANDAGE received FDA 510(k) clearance on 2009-07-31, under 510(k) number K083913.

Who is the listed applicant for CHESSON LABS 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 CHESSON LABS LIQUID BANDAGE?

The FDA product code for CHESSON LABS 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.

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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.

K120059LIQUID BANDAGE

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.

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLCK171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLCK120059LIQUID BANDAGEChesson Laboratory Associates, Inc.

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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