510(k) K842364

HANDHELD PACEMAKER PROGRAMMER & SOFTWAR by Cardiac Pacemakers, Inc. — Product Code KRG

K842364 is an FDA 510(k) premarket notification submitted by Cardiac Pacemakers, Inc. for the device "HANDHELD PACEMAKER PROGRAMMER & SOFTWAR". The FDA issued a decision of Substantially Equivalent on September 24, 1984. 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
September 24, 1984
Date Received
June 18, 1984
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