The following data is part of a premarket notification filed by Vascular Products, Inc. with the FDA for Vascular Biopsy Forceps.
| Device ID | K910840 |
| 510k Number | K910840 |
| Device Name: | VASCULAR BIOPSY FORCEPS |
| Classification | Device, Biopsy, Endomyocardial |
| Applicant | VASCULAR PRODUCTS, INC. 1316 BELECHER DR. N Tarpon Springs, FL 34689 |
| Contact | Patrick J Lamb |
| Correspondent | Patrick J Lamb VASCULAR PRODUCTS, INC. 1316 BELECHER DR. N Tarpon Springs, FL 34689 |
| Product Code | DWZ |
| CFR Regulation Number | 870.4075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-02-27 |
| Decision Date | 1991-07-15 |