Cardiac Pacemakers, Inc. - FDA 510(k) Cleared Devices
76
Total
76
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cardiac Pacemakers, Inc. Cardiovascular ✕
63 devices
Cleared
Mar 05, 2010
ACUITY BREAK-AWAY GUIDE CATHETER
Cardiovascular
72d
Cleared
Mar 20, 2008
ACUITY UNIVERSAL CUTTER
Cardiovascular
57d
Cleared
Jan 10, 1994
REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER
Cardiovascular
101d
Cleared
Oct 28, 1992
ASTRA T2, ASTRA T4, ASTRA T6
Cardiovascular
260d
Cleared
Jun 17, 1991
PDT CARRYALL TRANSMITTER, VARIOUS MODELS
Cardiovascular
19d
Cleared
Jan 30, 1991
LEAD STYLET
Cardiovascular
43d
Cleared
Sep 13, 1989
MODEL 6888 LEAD TUNNELER
Cardiovascular
48d
Cleared
Mar 10, 1989
ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE
Cardiovascular
23d
Cleared
Jan 27, 1988
TORQUE HEX WRENCH
Cardiovascular
43d
Cleared
Feb 19, 1987
ASTRA T2, T4 AND T6
Cardiovascular
58d
Cleared
Dec 05, 1986
ULTRA SOFTWARE MODULE: MODEL 2016
Cardiovascular
115d
Cleared
Sep 29, 1986
PROGRAMMER MODEL 2035/ELECTROGRAM CABLE MODEL 6580
Cardiovascular
48d
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