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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