The following data is part of a premarket notification filed by Cook Urological, Inc. with the FDA for Cook Ivf Cryopreservation Kit And The Cook Ivf Thaw Kit.
| Device ID | K011157 |
| 510k Number | K011157 |
| Device Name: | COOK IVF CRYOPRESERVATION KIT AND THE COOK IVF THAW KIT |
| Classification | Media, Reproductive |
| Applicant | COOK UROLOGICAL, INC. 1100 WEST MORGAN ST. P.O. BOX 227 Spencer, IN 47460 |
| Contact | Brenda Davis |
| Correspondent | Brenda Davis COOK UROLOGICAL, INC. 1100 WEST MORGAN ST. P.O. BOX 227 Spencer, IN 47460 |
| Product Code | MQL |
| CFR Regulation Number | 884.6180 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-04-16 |
| Decision Date | 2001-05-03 |