Medical Device Manufacturer · US , Woodstock , IL

Avitro, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2000
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Avitro, LLC General Hospital ✕

2 devices
1-2 of 2
Cleared Oct 19, 2000
0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE
K000632 · FOZ
General Hospital · 238d
Cleared Oct 19, 2000
THE AVITRO LLC, 10 AND 100 USO UNITS/ML HEPARIN SODIUM VAFD
K001795 · FOZ
General Hospital · 127d
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