510(k) K811217

PACEMAKER PROGRAMMER #2010 by Cardiac Pacemakers, Inc. — Product Code KRG

K811217 is an FDA 510(k) premarket notification submitted by Cardiac Pacemakers, Inc. for the device "PACEMAKER PROGRAMMER #2010". The FDA issued a decision of Substantially Equivalent on July 20, 1981. The device falls under product code KRG (Programmer, Pacemaker), a Class III device regulated under 21 CFR 870.3700. Cardiac Pacemakers, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 20, 1981
Date Received
May 4, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Programmer, Pacemaker
Device Class
Class III
Regulation Number
870.3700
Review Panel
CV
Submission Type