510(k) K854132

COOK PACEMAKER 332T, SERIES R BIPOLAR CARDIAC PULS by Cook Pacemaker Corp. — Product Code DXY

K854132 is an FDA 510(k) premarket notification submitted by Cook Pacemaker Corp. for the device "COOK PACEMAKER 332T, SERIES R BIPOLAR CARDIAC PULS". The FDA issued a decision of Substantially Equivalent on December 3, 1985. The device falls under product code DXY (Implantable Pacemaker Pulse-Generator), a Class III device regulated under 21 CFR 870.3610. Cook Pacemaker Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 3, 1985
Date Received
October 10, 1985
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