K991346 is an FDA 510(k) clearance for the PH-100, MODEL 2104. This device is classified as a Media, Reproductive (Class II - Special Controls, product code MQL).
Submitted by Vitrolife Sweden AB (Gothenberg, SE). The FDA issued a Cleared decision on February 24, 2000, 311 days after receiving the submission on April 19, 1999.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.6180.
| 510(k) Number | K991346 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 19, 1999 |
| Decision Date | February 24, 2000 |
| Days to Decision | 311 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 |