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

AIA-PACK T4

K Number: K896982 · Decision Mar 9, 1990
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
85
Applicant Total
11
Review Days
80

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Basic Information

Device Name
AIA-PACK T4
K Number
K896982
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1700
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Tosoh Corp.
Date Received
December 19, 1989
Decision Date
March 9, 1990
Product Code
KLI
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
KLI Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine

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Other Clearances by Tosoh Corp.

K Number Device Name
K023240 ST AIA-PACK CA 19-9
K023239 AIA-PACK CA 19-9
K923021 AIA-1200DX - AUTOMATED ENZYME IMMUNOASSAY SYSTEM
K913663 AIA-PACK T-U
K913298 AIA-PACK CK-MB
K913493 AIA-PACK FT4
K903628 AIA-PACK IRI
K901965 MPR-4A - MICRO-PLATE READER
K901674 AIA-600 AUTOMATED ENZYME IMMUNOASSAY SYSTEM
K897001 TOSOH AIA-PACK T3
Search all 11 clearances from Tosoh Corp. →