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

DEHYDROEPIANDROSTERONE SULFATE KIT RIA

K Number: K802195 · Decision Oct 23, 1980
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
27
Applicant Total
15
Review Days
43

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Basic Information

Device Name
DEHYDROEPIANDROSTERONE SULFATE KIT RIA
K Number
K802195
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1245
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Radioassay Systems Laboratories, Inc.
Date Received
September 10, 1980
Decision Date
October 23, 1980
Product Code
JKC
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
JKC Radioimmunoassay, Dehydroepiandrosterone (Free And Sulfate)

Similar 510(k) Clearances

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

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Other Clearances by Radioassay Systems Laboratories, Inc.

K Number Device Name
K862204 RSL (125I) ALDOSTERONE KIT
K842960 ANDROSTENEDIONE BY RIA
K840886 HYDROXYPROGESTERONE BY RIA 17A
K831855 HATCH KIT
K800126 RSL (125 L) PROGESTERONE KIT
K791999 (125I) TESTOSTERONE KIT
K791651 TOTAL ESTROGENS KIT BY RIA
K791728 RSL'S ASSAY PROCEDURE QUANTITATION
K791740 SERUM 11-DESOXYCORTISOL I AS TRACER
K791835 CORALENT COAT 125I CORTISOL RADIOIMM.
Search all 15 clearances from Radioassay Systems Laboratories, Inc. →