The following data is part of a premarket notification filed by Cook Urological, Inc. with the FDA for Coring Morcellator.
| Device ID | K960262 |
| 510k Number | K960262 |
| Device Name: | CORING MORCELLATOR |
| Classification | Laparoscope, Gynecologic (and Accessories) |
| Applicant | COOK UROLOGICAL, INC. 1100 WEST MORGAN ST. P.O. BOX 227 Spencer, IN 47460 |
| Contact | Tammy Bacon |
| Correspondent | Tammy Bacon COOK UROLOGICAL, INC. 1100 WEST MORGAN ST. P.O. BOX 227 Spencer, IN 47460 |
| Product Code | HET |
| CFR Regulation Number | 884.1720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-18 |
| Decision Date | 1996-04-15 |
| Summary: | summary |