The following data is part of a premarket notification filed by Cook Urological, Inc. with the FDA for Aq Hydrophilic Dilators.
| Device ID | K961904 |
| 510k Number | K961904 |
| Device Name: | AQ HYDROPHILIC DILATORS |
| Classification | Dilator, Urethral |
| 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 | KOE |
| CFR Regulation Number | 876.5520 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-05-16 |
| Decision Date | 1996-10-18 |
| Summary: | summary |