Medical Device Manufacturer · US , Northport , NY

Cortronic Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1986
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Cortronic Corp. Cardiovascular ✕

2 devices
1-2 of 2
Cleared Jan 13, 1989
CORTRONIC SCR1000
K884911 · DSF
Cardiovascular · 49d
Cleared Nov 10, 1986
CORTRONIC APM 770 NONINVASIVE & ARTERIAL PRESS MON
K852547 · DQO
Cardiovascular · 514d
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