Rapid Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rapid Diagnostics, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Rapid Diagnostics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Burlingame, US.
Historical record: 4 cleared submissions from 1998 to 2004. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Rapid Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rapid Diagnostics, Inc.
4 devices
Cleared
May 17, 2004
MICROMEDIC DRUGS OF ABUSE PANEL TEST (9), CATALOG NUMBER 07RD-7062
Toxicology
187d
Cleared
May 06, 2002
RAPID OPIATES TEST STRIP II, RAPID OPIATES TEST CARD II AND DOA MULTIPLE DRUG...
Toxicology
62d
Cleared
Apr 20, 2001
RAPID DRUGS OF ABUSE SINGLE AND MULTIPLE TEST PANELS
Toxicology
133d
Cleared
Jun 05, 1998
RAPIDHCG PREGNANCY TEST
Chemistry
17d