The following data is part of a premarket notification filed by Wilson-cook Medical, Inc. with the FDA for Balloon Dilation Catheter.
| Device ID | K935094 |
| 510k Number | K935094 |
| Device Name: | BALLOON DILATION CATHETER |
| Classification | Stents, Drains And Dilators For The Biliary Ducts |
| Applicant | WILSON-COOK MEDICAL, INC. 4900 BETHANIA STATION RD. & 5951 GRASSY CREEK BLVD. Winston-salem, NC 27105 |
| Contact | Paula A Joyce |
| Correspondent | Paula A Joyce WILSON-COOK MEDICAL, INC. 4900 BETHANIA STATION RD. & 5951 GRASSY CREEK BLVD. Winston-salem, NC 27105 |
| Product Code | FGE |
| CFR Regulation Number | 876.5010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-10-22 |
| Decision Date | 1995-01-24 |