Medical Device Manufacturer · IT , Mirandola ( Modena)

Dideco - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995
5
Total
5
Cleared
0
Denied

FDA 510(k) Regulatory Record - Dideco Cardiovascular ✕

3 devices
1-3 of 3
Cleared Oct 04, 2001
MONOLYTH MIMESYS HOLLOW FIBER OXYGENATOR
K004001 · DTZ
Cardiovascular · 282d
Cleared Sep 27, 2001
DIDECO D901 LILLIPUT HOLLOW FIBER OXYGENATOR WITH OR WITHOUT SOFT VENOUS...
K010478 · DTZ
Cardiovascular · 219d
Cleared Jul 28, 2000
DATA MASTER PERFUSION MONITORING SYSTEM
K001388 · DRY
Cardiovascular · 87d
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All5 Cardiovascular 3 Anesthesiology 2