K171148 is an FDA 510(k) clearance for the Aleo BME Liquid Bandage, a Bandage, Liquid (Class I — General Controls, product code KMF), submitted by Aleo Bme, Inc. (State College, US). The FDA issued a Cleared decision on January 12, 2018, 268 days after receiving the submission on April 19, 2017. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 880.5090.
| 510(k) Number | K171148 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 19, 2017 |
| Decision Date | January 12, 2018 |
| Days to Decision | 268 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | KMF — Bandage, Liquid |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 880.5090 |