Verichem Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Verichem Laboratories, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Verichem Laboratories, Inc. has 14 FDA 510(k) cleared chemistry devices. Based in East Providence, US.
Historical record: 14 cleared submissions from 1988 to 2012.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Verichem Laboratories, Inc.
14 devices
Cleared
Mar 28, 2012
MULTI-CHEMISTRY STANDARD KIT, URIC ACID STANDARD KIT, URINE CHEMISTRY...
Chemistry
182d
Cleared
Dec 19, 1997
MICROPROTEIN STANDARD KIT
Chemistry
35d
Cleared
Oct 29, 1997
MATRIX PLUS MULTI-CALIBRATOR KIT
Chemistry
54d
Cleared
Jul 23, 1997
AMMONIA/IRON STANDARD KIT
Chemistry
30d
Cleared
Jan 13, 1993
HDL-CHOLESTEROL STANDARD, MODIFICATION
Chemistry
106d
Cleared
Jul 19, 1991
ELECTROLYTE CONTROL
Chemistry
43d
Cleared
Mar 29, 1990
MATRIX PLUS(TM) CHEMISTRY REFERENCE STANDARD
Chemistry
22d
Cleared
Oct 25, 1988
BILIRUBIN STANDARD
Chemistry
162d
Cleared
Sep 09, 1988
URINE TOXICOLOGY STANDARD
Toxicology
165d
Cleared
Sep 02, 1988
MULTI-CHEMISTRY LINEARITY STANDARD
Chemistry
248d
Cleared
Aug 04, 1988
ETHYL ALCOHOL STANDARD
Toxicology
77d
Cleared
Jun 24, 1988
TOTAL PROTEIN/ALBUMIN STANDARD
Chemistry
36d
Cleared
May 31, 1988
THERAPEUTIC DRUG STANDARD
Toxicology
99d
Cleared
Feb 18, 1988
MULTI-ENZYME LINEARITY SOLUTION
Chemistry
27d