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

MODIFIED LH ENZYME IMMUNOASSAY TEST KIT

K Number: K896642 · Decision Jan 30, 1990
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
142
Applicant Total
39
Review Days
67

Basic Information

Device Name
MODIFIED LH ENZYME IMMUNOASSAY TEST KIT
K Number
K896642
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1485
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
MEDIX BIOTECH, INC.
Date Received
November 24, 1989
Decision Date
January 30, 1990
Product Code
CEP
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
CEP Radioimmunoassay, Luteinizing Hormone

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