The following data is part of a premarket notification filed by Valley Forge Scientific Corp. with the FDA for Mini-symm Bipolar Coagulator.
Device ID | K964143 |
510k Number | K964143 |
Device Name: | MINI-SYMM BIPOLAR COAGULATOR |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | VALLEY FORGE SCIENTIFIC CORP. 136 GREEN TREE RD. P.O. BOX 1179 Oaks, PA 19456 |
Contact | Jerry L Malis |
Correspondent | Jerry L Malis VALLEY FORGE SCIENTIFIC CORP. 136 GREEN TREE RD. P.O. BOX 1179 Oaks, PA 19456 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-10-17 |
Decision Date | 1997-01-09 |
Summary: | summary |