FDA 510(k) Applications Submitted by MEDPRO SAFETY PRODUCTS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K072602 | 09/14/2007 | VACUETTE PREMIUM SAFETY NEEDLE SYSTEM | MEDPRO SAFETY PRODUCTS, INC. |
| K102010 | 07/16/2010 | VACUETTE PREMIUM SAFETY BLOOD COLLECTION SET | MEDPRO SAFETY PRODUCTS, INC. |
| K111424 | 05/23/2011 | VACUETTE PREMIUM SAFETY NEEDLE SYSTEM TUBE-TOUCH | MEDPRO SAFETY PRODUCTS, INC. |
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