The following data is part of a premarket notification filed by Valley Forge Scientific Corp. with the FDA for Malis Bipolar Electrosurgical System Cmc-iii.
Device ID | K896541 |
510k Number | K896541 |
Device Name: | MALIS BIPOLAR ELECTROSURGICAL SYSTEM CMC-III |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | VALLEY FORGE SCIENTIFIC CORP. P.O. BOX 925 Valley Forge, PA 19482 |
Contact | Jerry L Malis |
Correspondent | Jerry L Malis VALLEY FORGE SCIENTIFIC CORP. P.O. BOX 925 Valley Forge, PA 19482 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-11-15 |
Decision Date | 1990-01-29 |