FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ACTIVE CORTISOL DSL 2000-SP

K Number: K850141 · Decision Feb 6, 1985
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
83
Applicant Total
94
Review Days
23

Basic Information

Device Name
ACTIVE CORTISOL DSL 2000-SP
K Number
K850141
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1205
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
DIAGNOSTIC SYSTEMS LABORATORIES, INC.
Date Received
January 14, 1985
Decision Date
February 6, 1985
Product Code
CGR
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
CGR Radioimmunoassay, Cortisol

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