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FDA 510(k)

BAND-AID(R) BRAND LIQUID BANDAGE

K-Number: K062602 · 2006-12-11

ApplicantJohnson & Johnson Consumer Companies, Inc.
Decision Date2006-12-11
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BAND-AID(R) BRAND LIQUID BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Consumer Companies, Inc.. It received FDA 510(k) clearance on 2006-12-11 under 510(k) number K062602. 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 BAND-AID(R) BRAND LIQUID BANDAGE?

BAND-AID(R) BRAND LIQUID BANDAGE is a medical device that received FDA 510(k) clearance on 2006-12-11. The listed applicant is Johnson & Johnson Consumer Companies, Inc.. The 510(k) number is K062602.

When did BAND-AID(R) BRAND LIQUID BANDAGE receive FDA 510(k) clearance?

BAND-AID(R) BRAND LIQUID BANDAGE received FDA 510(k) clearance on 2006-12-11, under 510(k) number K062602.

Who is the listed applicant for BAND-AID(R) BRAND LIQUID BANDAGE?

The FDA 510(k) record lists Johnson & Johnson Consumer Companies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAND-AID(R) BRAND LIQUID BANDAGE?

The FDA product code for BAND-AID(R) BRAND 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 Johnson & Johnson Consumer Companies, 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.

K001023FREEDOM, MODEL 4660

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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