K181206 is an FDA 510(k) clearance for the GentleCath Glide Intermittent Urinary Catheter, a Catheter, Urethral (Class II — Special Controls, product code GBM), submitted by Convatec Limited (Deeside, GB). The FDA issued a Cleared decision on August 16, 2018, 101 days after receiving the submission on May 7, 2018. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5130.
| 510(k) Number | K181206 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | May 07, 2018 |
| Decision Date | August 16, 2018 |
| Days to Decision | 101 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | GBM — Catheter, Urethral |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.5130 |