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FDA 510(k)

Aleo BME Liquid Bandage

K-Number: K171148 · 2018-01-12

ApplicantAleo Bme, Inc.
Decision Date2018-01-12
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Aleo BME Liquid Bandage is the device name listed in this FDA 510(k) record. The listed applicant is Aleo Bme, Inc.. It received FDA 510(k) clearance on 2018-01-12 under 510(k) number K171148. 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 Aleo BME Liquid Bandage?

Aleo BME Liquid Bandage is a medical device that received FDA 510(k) clearance on 2018-01-12. The listed applicant is Aleo Bme, Inc.. The 510(k) number is K171148.

When did Aleo BME Liquid Bandage receive FDA 510(k) clearance?

Aleo BME Liquid Bandage received FDA 510(k) clearance on 2018-01-12, under 510(k) number K171148.

Who is the listed applicant for Aleo BME Liquid Bandage?

The FDA 510(k) record lists Aleo Bme, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Aleo BME Liquid Bandage?

The FDA product code for Aleo BME Liquid Bandage is KMF.

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, LLCK153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLC

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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