K193285 is an FDA 510(k) clearance for the V-ONESTEP. This device is classified as a Media, Reproductive (Class II — Special Controls, product code MQL).
Submitted by Vitromed GmbH (Jena, DE). The FDA issued a Cleared decision on November 20, 2020, 359 days after receiving the submission on November 27, 2019.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.6180.
| 510(k) Number | K193285 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 27, 2019 |
| Decision Date | November 20, 2020 |
| Days to Decision | 359 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | MQL — Media, Reproductive |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 884.6180 |