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FDA 510(k) Applications Submitted by MEDPRO TECHNOLOGIES, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K000369
02/04/2000
VACUFLOW+ BLOOD COLLECTION SET, MODEL 52221/3/5; VACUFLOW+ WITH HOLDER BLOOD COLLECTION SET, MODEL 82021/3/5 WITH HOLDER
MEDPRO TECHNOLOGIES, INC.
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