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FDA 510(k) Applications Submitted by JOHN B HOWELL
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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