FDA 510(k) Applications Submitted by ANTHONY J DIMONTE

FDA 510(k) Number Submission Date Device Name Applicant
K880266 01/22/1988 MULTI-ENZYME LINEARITY SOLUTION VERICHEM LABORATORIES, INC.
K880705 02/22/1988 THERAPEUTIC DRUG STANDARD VERICHEM LABORATORIES, INC.
K901113 03/07/1990 MATRIX PLUS(TM) CHEMISTRY REFERENCE STANDARD VERICHEM LABORATORIES, INC.
K881320 03/28/1988 URINE TOXICOLOGY STANDARD VERICHEM LABORATORIES, INC.
K882059 05/16/1988 BILIRUBIN STANDARD VERICHEM LABORATORIES, INC.
K882116 05/19/1988 TOTAL PROTEIN/ALBUMIN STANDARD VERICHEM LABORATORIES, INC.
K882117 05/19/1988 ETHYL ALCOHOL STANDARD VERICHEM LABORATORIES, INC.
K912513 06/06/1991 ELECTROLYTE CONTROL VERICHEM LABORATORIES, INC.
K972333 06/23/1997 AMMONIA/IRON STANDARD KIT VERICHEM LABORATORIES, INC.
K973345 09/05/1997 MATRIX PLUS MULTI-CALIBRATOR KIT VERICHEM LABORATORIES, INC.
K924904 09/29/1992 HDL-CHOLESTEROL STANDARD, MODIFICATION VERICHEM LABORATORIES, INC.
K974290 11/14/1997 MICROPROTEIN STANDARD KIT VERICHEM LABORATORIES, INC.
K875285 12/29/1987 MULTI-CHEMISTRY LINEARITY STANDARD VERICHEM LABORATORIES, INC.
K112834 09/28/2011 MULTI-CHEMISTRY STANDARD KIT, URIC ACID STANDARD KIT, URINE CHEMISTRY STARDAND KIT, URINE URIC ACID STANDARD KIT, CHOLES VERICHEM LABORATORIES, INC.


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