510(k) K864712

MODEL 1740 PERSONAL POCKET PROGRAMMER by Telectronics, Inc. — Product Code KRG

K864712 is an FDA 510(k) premarket notification submitted by Telectronics, Inc. for the device "MODEL 1740 PERSONAL POCKET PROGRAMMER". The FDA issued a decision of Substantially Equivalent on December 17, 1987. The device falls under product code KRG (Programmer, Pacemaker), a Class III device regulated under 21 CFR 870.3700. Telectronics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 17, 1987
Date Received
December 3, 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