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

ALLEGRO INTACT PARATHYROID HORMONE IMMUNOASSAY

K Number: K861797 · Decision Jul 22, 1986
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
85
Applicant Total
68
Review Days
74

Basic Information

Device Name
ALLEGRO INTACT PARATHYROID HORMONE IMMUNOASSAY
K Number
K861797
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1545
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
NICHOLS INSTITUTE DIAGNOSTICS
Date Received
May 9, 1986
Decision Date
July 22, 1986
Product Code
CEW
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
CEW Radioimmunoassay, Parathyroid Hormone

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K042689 NICHOLS ADVANTAGE CORTISOL
K040813 NICHOLS ADVANTAGE CHEMILUMINESCENCE INTACT PARATHYROID HORMONE, MODEL 62-7022
K033727 NICHOLS ADVANTAGE BIO-INTACT PTH (1-84) IMMUNOASSAY
K033302 NICHOLS ADVANTAGE BIO-INTACT PTH (1-84) ASSAY, MODEL 62-7040
K032188 NICHOLS ADVANTAGE ALDOSTERONE ASSAY
K022356 NICHOLS ADVANTAGE CHEMILUMINESCENCE HELICOBACTOR PYLORI IGG ANTIBODIES IMMUNOASSAY
K022472 PARATHYROID HORMONE TEST SYSTEM/NICHOLS ADVANTAGE QUICK-INTRAOPERATIVE BIO-INTACT PTH (1-84)
K013992 NICHOLS ADVANTAGE CHEMILUMINESCENCE BIO-INTACT PARATHYROID HORMONE (1-84) IMMUNOASSAY
Search all 68 clearances from NICHOLS INSTITUTE DIAGNOSTICS →