Medical Device Manufacturer · US , Mchenry , IL

Diagnostica, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1978

Total

Cleared

Denied

Diagnostica, Inc. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1978 to 2001. Primary specialty: Immunology.

Browse the FDA 510(k) cleared devices submitted by Diagnostica, Inc. Filter by specialty or product code using the sidebar.

Diagnostica, 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 - Diagnostica, Inc.

12 devices

1-12 of 12

H. INFLUENZA B ANTISERA FOR CIE

K823348 · GRP

Immunology · 49d

Cleared Sep 23, 1981

DIAGNOSTIC KITS & KIT COMPONENTS

K812434 · LHT

Microbiology · 29d

Cleared Mar 12, 1980

PARACONTROL ABNORMAL IMMUNOGLOBULIN CONT

ANTI-HUMAN LAMBDA SERUM

K791283 · DEH

Immunology · 140d

Cleared Nov 27, 1979

ANTI-HUMAN KAPPA SERUM

ASPERGILLUS FUMIGATUS, ASPERGILLUS FLAVU

K790672 · JWT

Microbiology · 55d

Cleared Oct 24, 1978

BUFFER, COLLAGEN REAGENT AND DILUENT

K781710 · JBX

Hematology · 19d

Diagnostica, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Diagnostica, Inc.

Filters