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FDA 510(k) Applications Submitted by REMEL CO.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K960090
01/11/1996
CALCOFLUOR WHITE STAIN KIT
REMEL CO.
K955669
12/13/1995
REMEL CEFEPIME 30 UG SUSCEPTIBILITY DISK
REMEL CO.
K965149
12/23/1996
A.C.T. I
REMEL CO.
K965150
12/23/1996
A.C.T. IV
REMEL CO.
K965151
12/23/1996
A.C.T. III
REMEL CO.
K965152
12/23/1996
A.C.T. II
REMEL CO.
K960095
01/11/1996
BACTIDROP CALCOFLUOR WHITE
REMEL CO.
K013711
11/07/2001
BACTI-SWAB DRY
REMEL CO.
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