510(k) K953417

MINIFLEX MODEL 340, 341, AND 342 PULSE GENERATORS by Cook Pacemaker Corp. — Product Code DXY

K953417 is an FDA 510(k) premarket notification submitted by Cook Pacemaker Corp. for the device "MINIFLEX MODEL 340, 341, AND 342 PULSE GENERATORS". The FDA issued a decision of ST on September 29, 1995. 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
ST ()
Decision Date
September 29, 1995
Date Received
June 8, 1995
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