Medical Device Manufacturer · US , Lexington , KY

Medpro Safety Products, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2008

Recent clearances: VACUETTE PREMIUM SAFETY NEEDLE SYSTEM TUBE-TOUCH, VACUETTE PREMIUM SAFETY BLOOD COLLECTION SET, VACUETTE PREMIUM SAFETY NEEDLE SYSTEM

View 3 510(k) Devices ↓
3
Total
3
Cleared
0
Denied

FDA 510(k) Regulatory Record - Medpro Safety Products, Inc. General Hospital ✕

3 devices
1-3 of 3
Cleared Jul 29, 2011
VACUETTE PREMIUM SAFETY NEEDLE SYSTEM TUBE-TOUCH
K111424 · FMI
General Hospital · 67d
Cleared Nov 19, 2010
VACUETTE PREMIUM SAFETY BLOOD COLLECTION SET
K102010 · FMI
General Hospital · 126d
Cleared Jun 18, 2008
VACUETTE PREMIUM SAFETY NEEDLE SYSTEM
K072602 · FMI
General Hospital · 278d
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