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

INSULIN-LIKE GROWTH FACTOR I (IGF-I), IMMUNORADIOMETERIC ASSAY (IRMA)

K Number: K952505 · Decision Jul 3, 1995
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
35
Applicant Total
15
Review Days
33

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Basic Information

Device Name
INSULIN-LIKE GROWTH FACTOR I (IGF-I), IMMUNORADIOMETERIC ASSAY (IRMA)
K Number
K952505
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1370
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nichols Institute
Date Received
May 31, 1995
Decision Date
July 3, 1995
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CFL), ordered by most recent decision date.

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Other Clearances by Nichols Institute

K Number Device Name
K952559 ERYTHROPOIETIN IMMUNOASSAY KIT
K946247 IGFBP-3; INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN-3
K950524 NICHOLS INSTITUTE DIAGNOSTICS DHEA-S CHEMILUMINESCENCE IMMUNOASSAY
K932650 ERYTHROPOIETIN IMMUNOASSAY KIT
K931600 CHEMILUMINESCENCE FREE T3 IMMUNOASSAY
K931777 APO A-1 CHEMILUMINESCENCE ASSAY
K931601 CHEMILUMINESCENCE DHEA-S IMMUNOASSAY
K926396 ADRENOCORTICOTROPIC/ACTH ANALYSIS PRODUCT
K931311 THYROID PEROXIDASE AUTO ANTIBODIES(TPO) IMMUN KIT
K930777 THYROGLOBULIN AUTOANTIBODY IMMUNOASSAY KIT
Search all 15 clearances from Nichols Institute →