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

DHEA-SULFATE TEST SET

K Number: K792041 · Decision Oct 30, 1979
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
27
Applicant Total
13
Review Days
18

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Basic Information

Device Name
DHEA-SULFATE TEST SET
K Number
K792041
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1245
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Wien Laboratories, Inc.
Date Received
October 12, 1979
Decision Date
October 30, 1979
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)

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Other Clearances by Wien Laboratories, Inc.

K Number Device Name
K912850 SHBG
K834246 PROGESTERONE TEST SET 125I 17-OH
K832452 ANDROSTENEDIONE TEST SET 125I
K823200 125 I-DEHYDROEPIANDROSTERONE SULFATE
K821653 PROTRIPTYLINE TRI-CY TEST SET
K821652 DOXEPIN TRI-CY TEST SET
K802728 125I-TESTOSTERONE TEST SET
K781834 TEST SET, 125 I-DIGOXIN
K781599 I-ESTRIOL TEST SET
K772306 125I DIGOXIN TEST SET
Search all 13 clearances from Wien Laboratories, Inc. →