Medac, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medac, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Medac, Inc. has 10 FDA 510(k) cleared cardiovascular devices. Based in Tualatin, US.
Historical record: 10 cleared submissions from 1987 to 1988.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medac, Inc.
10 devices
Cleared
Mar 07, 1988
MONITOR, ELECTROGRAPHIC
Cardiovascular
138d
Cleared
Jan 27, 1988
DISPOSABLE GEL DEFIBRILLATION/EXTERNAL PACING ELEC
Cardiovascular
91d
Cleared
Dec 15, 1987
300M ECG MONITRO/TRANSCUTANEOUS PACEMAKER
Cardiovascular
69d
Cleared
Nov 23, 1987
360D DC DEFIBRILLATOR
Cardiovascular
47d
Cleared
Apr 23, 1987
PACE 10 NON-INVASIVE EXTERNAL PACEMAKER
Cardiovascular
30d
Cleared
Mar 10, 1987
DISPOS GEL EXTERNAL PACING ELECTRODE/LOW IMPEDANCE
Cardiovascular
78d
Cleared
Mar 03, 1987
ETP 300 NON-INVASIVE EXTERNAL PACEMAKER
Cardiovascular
71d
Cleared
Mar 03, 1987
DISPOS GEL EXTERNAL PACING ELECTRODE/HI IMPEDANCE
Cardiovascular
71d
Cleared
Mar 03, 1987
ETP 180E NON-INVASIVE EXTERNAL PACEMAKER
Cardiovascular
71d
Cleared
Mar 03, 1987
ETP 180A NON-INVASIVE EXTERNAL PACEMAKER
Cardiovascular
71d