The following data is part of a premarket notification filed by Biosearch Medical Products, Inc. with the FDA for Dobbhoff(r) Percutaneous Transhepat Biliary Stent.
| Device ID | K913073 |
| 510k Number | K913073 |
| Device Name: | DOBBHOFF(R) PERCUTANEOUS TRANSHEPAT BILIARY STENT |
| Classification | Stents, Drains And Dilators For The Biliary Ducts |
| Applicant | BIOSEARCH MEDICAL PRODUCTS, INC. 35 INDUSTRIAL PKWY. P.O. BOX 1700 Somerville, NJ 08876 |
| Contact | Louis P Goodman |
| Correspondent | Louis P Goodman BIOSEARCH MEDICAL PRODUCTS, INC. 35 INDUSTRIAL PKWY. P.O. BOX 1700 Somerville, NJ 08876 |
| Product Code | FGE |
| CFR Regulation Number | 876.5010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-07-11 |
| Decision Date | 1991-10-25 |