FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TSH - THIRD GENERATION LOW CONTROLS

K Number: K924675 · Decision Nov 18, 1992
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
15
Review Days
63

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Basic Information

Device Name
TSH - THIRD GENERATION LOW CONTROLS
K Number
K924675
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nichols Institute
Date Received
September 16, 1992
Decision Date
November 18, 1992
Product Code
JJX
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

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K931777 APO A-1 CHEMILUMINESCENCE ASSAY
K931601 CHEMILUMINESCENCE DHEA-S IMMUNOASSAY
K926396 ADRENOCORTICOTROPIC/ACTH ANALYSIS PRODUCT
K931311 THYROID PEROXIDASE AUTO ANTIBODIES(TPO) IMMUN KIT
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