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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