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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 a medical device manufactured by Aleo Bme, Inc.. It received FDA 510(k) clearance on 2018-01-12 under approval 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. It is manufactured by Aleo Bme, Inc.. The 510(k) number is K171148.

When was Aleo BME Liquid Bandage approved by the FDA?

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

What company makes Aleo BME Liquid Bandage?

Aleo BME Liquid Bandage is manufactured by Aleo Bme, Inc..

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

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

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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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