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

ACS:180 BR (AUTOMATED CHEMILUMINESCENCE SYSTEM FOR THE QUANTITATION OF CANCER ANTIGEN 27.29)

K Number: K970695 · Decision Aug 8, 1997
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
27
Applicant Total
20
Review Days
164

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Basic Information

Device Name
ACS:180 BR (AUTOMATED CHEMILUMINESCENCE SYSTEM FOR THE QUANTITATION OF CANCER ANTIGEN 27.29)
K Number
K970695
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
February 25, 1997
Decision Date
August 8, 1997
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

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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
K982680 CHIRON DIAGNOSTICS CORPORATION ACS: CENTAUR BR IMMUNOASSAY
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
Search all 20 clearances from Chiron Diagnostics Corp. →