The following data is part of a premarket notification filed by Cook Ob/gyn with the FDA for Sydney Ivf Embryo Biopsy Medium.
| Device ID | K023850 |
| 510k Number | K023850 |
| Device Name: | SYDNEY IVF EMBRYO BIOPSY MEDIUM |
| Classification | Media, Reproductive |
| Applicant | COOK OB/GYN 1100 WEST MORGAN ST. P.O. BOX 271 Spencer, IN 47460 |
| Contact | Debbie Schmitt |
| Correspondent | Debbie Schmitt COOK OB/GYN 1100 WEST MORGAN ST. P.O. BOX 271 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 | 2002-11-19 |
| Decision Date | 2003-01-22 |
| Summary: | summary |