510(k) K872766

IMPLANTABLE PROGRAMMABLE CARDIAC PULSE GENERATORS by Telectronics, Inc. — Product Code DXY

K872766 is an FDA 510(k) premarket notification submitted by Telectronics, Inc. for the device "IMPLANTABLE PROGRAMMABLE CARDIAC PULSE GENERATORS". The FDA issued a decision of Substantially Equivalent on November 4, 1987. The device falls under product code DXY (Implantable Pacemaker Pulse-Generator), a Class III device regulated under 21 CFR 870.3610. Telectronics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 4, 1987
Date Received
July 14, 1987
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