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

17 B-ESTRADIOL (ELISA)

K Number: K973901 · Decision Nov 24, 1997
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
49
Applicant Total
6
Review Days
41

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Basic Information

Device Name
17 B-ESTRADIOL (ELISA)
K Number
K973901
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1260
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kmi Diagnostics, Inc.
Date Received
October 14, 1997
Decision Date
November 24, 1997
Product Code
CHP
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
CHP Radioimmunoassay, Estradiol

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Other Clearances by Kmi Diagnostics, Inc.

K Number Device Name
K010790 CORTISOL LIA
K990073 CALCITONIN
K973900 TESTOTERONE ELISA
K973898 PROGESTERONE ELISA
K973897 DHEA-S