The following data is part of a premarket notification filed by Cardiac Control Systems, Inc. with the FDA for Ccs Implantable Maestro 106/206/210 Cardiac Pacema.
Device ID | K853471 |
510k Number | K853471 |
Device Name: | CCS IMPLANTABLE MAESTRO 106/206/210 CARDIAC PACEMA |
Classification | Implantable Pacemaker Pulse-generator |
Applicant | CARDIAC CONTROL SYSTEMS, INC. 3 COMMERCE BLVD. Palm Coast, FL 32164 |
Contact | Kenneth J Durbin |
Correspondent | Kenneth J Durbin CARDIAC CONTROL SYSTEMS, INC. 3 COMMERCE BLVD. Palm Coast, FL 32164 |
Product Code | DXY |
CFR Regulation Number | 870.3610 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-08-19 |
Decision Date | 1986-02-24 |