K190620 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 July 10, 2019, 121 days after receiving the submission on March 11, 2019.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5130.
| 510(k) Number | K190620 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 11, 2019 |
| Decision Date | July 10, 2019 |
| Days to Decision | 121 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 |