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

AIA-PACK HGH

K Number: K905757 · Decision Jan 25, 1991
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
35
Applicant Total
41
Review Days
29

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Basic Information

Device Name
AIA-PACK HGH
K Number
K905757
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1370
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Tosoh Medics, Inc.
Date Received
December 27, 1990
Decision Date
January 25, 1991
Product Code
CFL
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
CFL Radioimmunoassay, Human Growth Hormone

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K Number Device Name
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K023091 ST AIA-PACK TESTOSTERONE ASSAY
K023891 ST AIA-PACK CA 125 ENZYME IMMUNOASSAY
K020489 G7 AUTOMATED HPLC ANALYZER, BETA-THALASSEMIA MODE
K012820 AIA-PACK CTNI 2ND-GEN ASSAY
K011434 G7 AUTOMATED HPLC ANALYZER
K010796 AIA-PACK BRCA, ST AIA PACK BRCA
K992365 AIA-PACK FOLATE ASSAY
K990431 AIA-PACK CA 125
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