K180070 is an FDA 510(k) clearance for the SpeediCath Flex Coude Pro. This device is classified as a Catheter, Urethral (Class II — Special Controls, product code GBM).
Submitted by Coloplast (Plymouth, US). The FDA issued a Cleared decision on February 2, 2018, 24 days after receiving the submission on January 9, 2018.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5130.
| 510(k) Number | K180070 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 09, 2018 |
| Decision Date | February 02, 2018 |
| Days to Decision | 24 days |
| Submission Type | Special |
| 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 |