Medical Device Manufacturer · US , Walker , MI

Diagnostic Reagents, Inc. - FDA 510(k) Cleared Devices

66 submissions · 66 cleared · Since 1982

Total

Cleared

Denied

Diagnostic Reagents, Inc. has 66 FDA 510(k) cleared toxicology devices. Based in Walker, US.

Historical record: 66 cleared submissions from 1982 to 1998.

Browse the complete list of FDA 510(k) cleared toxicology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Diagnostic Reagents, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Diagnostic Reagents, Inc.

66 devices

1-12 of 66

Cleared Nov 18, 1998

MODIFICATION OF TRICYCLIC SERUM TOX EIA ASSAY

DRUGS OF ABUSE URINE CALIBRATORS AND CONTROLS

50NG/ML COCAINE METABOLITE CALIBRATOR

QUINIDINE ENZYME IMMUNOASSAY

K964212 · LBZ

Toxicology · 57d

Cleared Dec 10, 1996

DIGOXIN ENZYME IMMUNOASSAY

K963835 · KXT

Toxicology · 77d

Cleared Aug 14, 1996

PROCAINAMIDE ENZYME IMMUNOASSAY

K962463 · LAR

Toxicology · 50d

Cleared Jul 16, 1996

VALPROIC ACID EIA TEST

K961988 · LEG

Toxicology · 56d

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Diagnostic Reagents, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Diagnostic Reagents, Inc.

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