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

CHIRON DIAGNOSTICS ACS:180TU P

K Number: K970539 · Decision Mar 24, 1997
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
92
Applicant Total
20
Review Days
40

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Basic Information

Device Name
CHIRON DIAGNOSTICS ACS:180TU P
K Number
K970539
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1715
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Chiron Diagnostics Corp.
Date Received
February 12, 1997
Decision Date
March 24, 1997
Product Code
KHQ
Advisory Committee
Clinical Chemistry
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
KHQ Radioassay, Triiodothyronine Uptake

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KHQ), 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
K974325 CHIRON DIAGNOSTICS ACS:180 MYOGLOBIN
Search all 20 clearances from Chiron Diagnostics Corp. →