The following data is part of a premarket notification filed by Unimed Surgical Products, Inc. with the FDA for Surgi-link Bipolar Micro Forceps.
Device ID | K946246 |
510k Number | K946246 |
Device Name: | SURGI-LINK BIPOLAR MICRO FORCEPS |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | UNIMED SURGICAL PRODUCTS, INC. 10401 BELCHER RD. Largo, FL 33777 |
Contact | Lorna K Linville |
Correspondent | Lorna K Linville UNIMED SURGICAL PRODUCTS, INC. 10401 BELCHER RD. Largo, FL 33777 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-12-22 |
Decision Date | 1995-03-07 |