510(k) K860584

SOFTWARE MODULE/2035 PROG AND ASTRA/T PULSE GEN by Cardiac Pacemakers, Inc. — Product Code KRG

K860584 is an FDA 510(k) premarket notification submitted by Cardiac Pacemakers, Inc. for the device "SOFTWARE MODULE/2035 PROG AND ASTRA/T PULSE GEN". The FDA issued a decision of Substantially Equivalent on June 6, 1986. 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
June 6, 1986
Date Received
February 18, 1986
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