FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CHIRON DIAGNOSTICS CORPORATION ACS: CENTAUR BR IMMUNOASSAY

K Number: K982680 · Decision Oct 15, 1998
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
27
Applicant Total
20
Review Days
76

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Basic Information

Device Name
CHIRON DIAGNOSTICS CORPORATION ACS: CENTAUR BR IMMUNOASSAY
K Number
K982680
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.6010
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Chiron Diagnostics Corp.
Date Received
July 31, 1998
Decision Date
October 15, 1998
Product Code
MOI
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MOI System, Test, Immunological, Antigen, Tumor

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MOI), ordered by most recent decision date.

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Other Clearances by Chiron Diagnostics Corp.

K Number Device Name
K992157 CHIRON DIAGNOSTICS ACS: 180 FERRITIN ASSAY
K991582 CHIRON DIAGNOSTICS ACS: 180 FOLATE
K991692 CHIRON DIAGNOSTICS ACS: 180 FT3
K981478 ACS:CENTAUR CEA
K981839 ACS:CENTAUR PSA2 IMMUNOASSAY
K981592 ACS:CENTAUR AFP
K980528 CHIRON DIAGNOSTICS ACS:180 TROPONIN I ASSAY (CTNI)
K974029 ACS TOBRAMYCIN
K974325 CHIRON DIAGNOSTICS ACS:180 MYOGLOBIN
K970695 ACS:180 BR (AUTOMATED CHEMILUMINESCENCE SYSTEM FOR THE QUANTITATION OF CANCER ANTIGEN 27.29)
Search all 20 clearances from Chiron Diagnostics Corp. →