Medical Device Manufacturer · US , Oldsmar , FL

Promedica, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004
Official Website
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Promedica, Inc. General Hospital ✕

2 devices
1-2 of 2
Cleared Mar 29, 2004
THE ULTRA SYSTEM
K032445 · KCT
General Hospital · 234d
Cleared Feb 13, 2004
THE ULTRA SYSTEM SP
K032813 · KCT
General Hospital · 157d
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