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

DHEA-S DIRECT RIA KIT

K Number: K842555 · Decision Aug 7, 1984
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
27
Applicant Total
15
Review Days
36

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Basic Information

Device Name
DHEA-S DIRECT RIA KIT
K Number
K842555
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1245
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Biotecx Laboratories, Inc.
Date Received
July 2, 1984
Decision Date
August 7, 1984
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 Biotecx Laboratories, Inc.

K Number Device Name
K982298 OPTICOAT T4 EIA KIT
K981824 OPTICOAT T3 EIA KIT
K895407 CORTISOL CLASP-BEAD EIA KIT
K893620 T3 CLASP-BEAD EIA KIT
K892853 T4 CLASP-BEAD EIA KIT
K883765 TBG 125I RIA KIT, RADIOIMMUNO. OF SERUM THYROXINE
K871211 PROGESTERONE CLASP RADIOIMMUNOASSAY KIT
K863188 HPL RIA KIT
K854876 ALDOSTERONE DIRECT RIA KIT
K851540 ESTRADIOL DIRECT RIA KIT
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