510(k) K905824

MAESTRO(R) SERIES 100/200 CARDIAC S/CHAMB PACEMAKE by Cardiac Control Systems, Inc. — Product Code DXY

K905824 is an FDA 510(k) premarket notification submitted by Cardiac Control Systems, Inc. for the device "MAESTRO(R) SERIES 100/200 CARDIAC S/CHAMB PACEMAKE". The FDA issued a decision of Substantially Equivalent on May 16, 1991. The device falls under product code DXY (Implantable Pacemaker Pulse-Generator), a Class III device regulated under 21 CFR 870.3610. Cardiac Control Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 16, 1991
Date Received
December 31, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Implantable Pacemaker Pulse-Generator
Device Class
Class III
Regulation Number
870.3610
Review Panel
CV
Submission Type