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

CHIRON DIAGNOSTICS ACS:180 MYOGLOBIN

K Number: K974325 · Decision Dec 8, 1997
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
45
Applicant Total
20
Review Days
20

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Basic Information

Device Name
CHIRON DIAGNOSTICS ACS:180 MYOGLOBIN
K Number
K974325
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5680
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Chiron Diagnostics Corp.
Date Received
November 18, 1997
Decision Date
December 8, 1997
Product Code
DDR
Advisory Committee
Immunology
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
DDR Myoglobin, Antigen, Antiserum, Control

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DDR), 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
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
K970695 ACS:180 BR (AUTOMATED CHEMILUMINESCENCE SYSTEM FOR THE QUANTITATION OF CANCER ANTIGEN 27.29)
Search all 20 clearances from Chiron Diagnostics Corp. →