K093273 is an FDA 510(k) clearance for the VIT KIT - FREEZE AND THAW, a Media, Reproductive (Class II — Special Controls, product code MQL), submitted by Irvine Scientific Sales Co., Inc. (Santa Ana, US). The FDA issued a Cleared decision on March 3, 2010, 135 days after receiving the submission on October 19, 2009. This device falls under the Obstetrics & Gynecology review panel. Regulated under 21 CFR 884.6180.
| 510(k) Number | K093273 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | October 19, 2009 |
| Decision Date | March 03, 2010 |
| Days to Decision | 135 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 |