FDA 510(k) Applications Submitted by BEMIS MFG. CO.

FDA 510(k) Number Submission Date Device Name Applicant
K960525 02/05/1996 BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100) BEMIS MFG. CO.
K020921 03/21/2002 NO-POKES NEEDLE SAFETY DEVICE BEMIS MFG. CO.
K964858 12/04/1996 BEMIS TWO GALLON CHEMOTHERAPY CONTAINER BEMIS MFG. CO.
K965248 12/04/1996 BEMIS TWO GALLON SHARPS CONTAINER BEMIS MFG. CO.


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