510(k) K841983

COOK PACEMAKER 216 BIPOLAR CARDIAC - by Cook Pacemaker Corp. — Product Code DXY

K841983 is an FDA 510(k) premarket notification submitted by Cook Pacemaker Corp. for the device "COOK PACEMAKER 216 BIPOLAR CARDIAC -". The FDA issued a decision of Substantially Equivalent on July 11, 1984. 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
July 11, 1984
Date Received
May 15, 1984
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