510(k) K853590

COOK PACEMAKER CORP. 327T, SERIES R UNIPOLAR CARDI by Cook Pacemaker Corp. — Product Code DXY

K853590 is an FDA 510(k) premarket notification submitted by Cook Pacemaker Corp. for the device "COOK PACEMAKER CORP. 327T, SERIES R UNIPOLAR CARDI". The FDA issued a decision of Substantially Equivalent on October 23, 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
October 23, 1985
Date Received
August 28, 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