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

MODIFIED COTROPIN RADIOIMMUNOASSAY KIT

K Number: K862180 · Decision Jul 7, 1986
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
142
Applicant Total
9
Review Days
28

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Basic Information

Device Name
MODIFIED COTROPIN RADIOIMMUNOASSAY KIT
K Number
K862180
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1485
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Clinetics Corp.
Date Received
June 9, 1986
Decision Date
July 7, 1986
Product Code
CEP
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
CEP Radioimmunoassay, Luteinizing Hormone

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Other Clearances by Clinetics Corp.

K Number Device Name
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K841580 TSH RECEPTOR ANTIBODY KIT 125I TSH
K833934 ADRENOCORTICOTROPIC HORMONE TEST
K830357 RADIOIMMUNOASSAY IMMUNOGLOBULINS D.E
K823379 125-I FSH RADIOIMMUNOASSAY KIT
K823380 125-I LH RADIOIMMUNOASSAY KIT
K822152 HCG BETA RIA KIT
K801306 CLINETICS PCA COLUMN