Medical Device Manufacturer · US , Medfield , MA

Chiron Diagnostics Corp. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1997

Total

Cleared

Denied

Chiron Diagnostics Corp. has 20 FDA 510(k) cleared medical devices. Based in Medfield, US.

Historical record: 20 cleared submissions from 1997 to 1999. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Chiron Diagnostics Corp. Filter by specialty or product code using the sidebar.

Chiron Diagnostics Corp. 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 - Chiron Diagnostics Corp.

20 devices

1-12 of 20

Cleared Aug 05, 1999

CHIRON DIAGNOSTICS ACS: 180 FERRITIN ASSAY

K992157 · DBF

Immunology · 41d

Cleared Jun 30, 1999

CHIRON DIAGNOSTICS ACS: 180 FOLATE

K991582 · CGN

Immunology · 54d

Cleared Jun 18, 1999

CHIRON DIAGNOSTICS ACS: 180 FT3

K991692 · CDP

Chemistry · 31d

Cleared Oct 15, 1998

CHIRON DIAGNOSTICS CORPORATION ACS: CENTAUR BR IMMUNOASSAY

ACS:CENTAUR PSA2 IMMUNOASSAY

CHIRON DIAGNOSTICS ACS:180 TROPONIN I ASSAY (CTNI)

CHIRON DIAGNOSTICS ACS:180 MYOGLOBIN

K974325 · DDR

Chemistry · 20d

Cleared Aug 08, 1997

ACS:180 BR (AUTOMATED CHEMILUMINESCENCE SYSTEM FOR THE QUANTITATION OF CANCER...

K970695 · MOI

Immunology · 164d

Cleared Jul 17, 1997

CHIRON DIAGNOSTICS AUTOMATED CHEMILUMINESCENCE SYSTEM (ASC) CENTAUR ANALYZER

K971418 · MOI

Chemistry · 92d

Chiron Diagnostics Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Chiron Diagnostics Corp.

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