510(k) K850656

COOK 331T UNIPOLAR CARDIAC PULSE GENERATOR W/TELEM by Cook Pacemaker Corp. — Product Code DXY

K850656 is an FDA 510(k) premarket notification submitted by Cook Pacemaker Corp. for the device "COOK 331T UNIPOLAR CARDIAC PULSE GENERATOR W/TELEM". The FDA issued a decision of Substantially Equivalent on March 1, 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
March 1, 1985
Date Received
February 19, 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