The following data is part of a premarket notification filed by Cardiothoracic Systems, Inc. with the FDA for Cts Midcab/svh Bipolar Scissors.
Device ID | K963930 |
510k Number | K963930 |
Device Name: | CTS MIDCAB/SVH BIPOLAR SCISSORS |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | CARDIOTHORACIC SYSTEMS, INC. 10600 NORTH TANTAU AVE. Cupertino, CA 95014 |
Contact | Michael J Billig |
Correspondent | Michael J Billig CARDIOTHORACIC SYSTEMS, INC. 10600 NORTH TANTAU AVE. Cupertino, CA 95014 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-10-01 |
Decision Date | 1997-01-16 |
Summary: | summary |