Rapid Diagnostic Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rapid Diagnostic Laboratories, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Rapid Diagnostic Laboratories, Inc. has 6 FDA 510(k) cleared medical devices. Based in Lakewood, US.
Historical record: 6 cleared submissions from 1985 to 1990. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Rapid Diagnostic Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rapid Diagnostic Laboratories, Inc.
6 devices
Cleared
Oct 26, 1990
BLIND CONTROLS FOR DRUGS OF ABUSE TESTING
Toxicology
65d
Cleared
Jan 23, 1989
NEW LOW LEVEL DRUG MIXTURE CONTROL
Toxicology
19d
Cleared
Jun 22, 1988
HIGH PERFORMANCE CALIBRATORS
Toxicology
183d
Cleared
Jul 07, 1987
HYPERFORMANCE CONTROLS (HP-CONTROLS)
Toxicology
70d
Cleared
Sep 25, 1986
HIGH PERFORMANCE CANNABINOID CONTROLS
Toxicology
42d
Cleared
Apr 10, 1985
COBE COP FILTER CARDIOPULMONARY PREBYPASS FILTER
Cardiovascular
86d