The following data is part of a premarket notification filed by Solco Basle, Inc. with the FDA for Hall Vein Stripper.
| Device ID | K872157 |
| 510k Number | K872157 |
| Device Name: | HALL VEIN STRIPPER |
| Classification | Stripper, Vein, External |
| Applicant | SOLCO BASLE, INC. POST OFFICE BOX 661 Wilton, CT 06897 |
| Contact | J Turner,phd |
| Correspondent | J Turner,phd SOLCO BASLE, INC. POST OFFICE BOX 661 Wilton, CT 06897 |
| Product Code | DWQ |
| CFR Regulation Number | 870.4885 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-06-04 |
| Decision Date | 1987-07-07 |