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

125I-TESTOSTERONE TEST SET

K Number: K802728 · Decision Dec 11, 1980
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
88
Applicant Total
13
Review Days
38

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Basic Information

Device Name
125I-TESTOSTERONE TEST SET
K Number
K802728
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1680
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Wien Laboratories, Inc.
Date Received
November 3, 1980
Decision Date
December 11, 1980
Product Code
CDZ
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
CDZ Radioimmunoassay, Testosterones And Dihydrotestosterone

Similar 510(k) Clearances

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

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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
K792041 DHEA-SULFATE 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. →