The following data is part of a premarket notification filed by Conway Stuart Medical, Inc. with the FDA for Electrosurgical Basket Electrodes Electrosurgical Basket Electrodes.
Device ID | K981589 |
510k Number | K981589 |
Device Name: | ELECTROSURGICAL BASKET ELECTRODES ELECTROSURGICAL BASKET ELECTRODES |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | CONWAY STUART MEDICAL, INC. 916 W. MAUDE AVE. Sunnyvale, CA 94086 |
Contact | Thomas Wehman |
Correspondent | Thomas Wehman CONWAY STUART MEDICAL, INC. 916 W. MAUDE AVE. Sunnyvale, CA 94086 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-05-04 |
Decision Date | 1998-07-30 |