KRG · Class III · 21 CFR 870.3700

FDA Product Code KRG: Programmer, Pacemaker

Leading manufacturers include Intermedics, Inc., Cordis Corp. and Medtronic Vascular.

25
Total
25
Cleared
132d
Avg days
1977
Since

FDA 510(k) Cleared Programmer, Pacemaker Devices (Product Code KRG)

25 devices
1–24 of 25
Cleared Mar 15, 1995
INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04
K933278
Intermedics, Inc.
Cardiovascular · 624d
Cleared Nov 17, 1988
MODEL 2331T PATIENT PROGRAMMER
K880738
Medtronic Vascular
Cardiovascular · 267d
Cleared Oct 27, 1981
INTERMEDICS PROGRAMMER, MODEL 522-03
K812813
Intermedics, Inc.
Cardiovascular · 21d
Cleared Mar 20, 1981
CORDIS PACEMAKER PROGRAMMERS 255A & 256A
K810552
Cordis Corp.
Cardiovascular · 18d
Cleared Nov 27, 1979
OMNICOR PROGRAMMER MODEL 222C
K791419
Cordis Corp.
Cardiovascular · 133d
Cleared Jul 31, 1979
PACEMAKER PROGRAMMER
K790220
Intermedics, Inc.
Cardiovascular · 182d
Cleared Apr 21, 1978
RATE PROGRAMMER MODEL 520
K780175
Intermedics, Inc.
Cardiovascular · 77d
Cleared Oct 07, 1977
OMNICOR PROGRAMMER MODEL 222A
K771855
Cordis Corp.
Cardiovascular · 9d

About Product Code KRG - Regulatory Context