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

TANDEMR M-PAK LH IMMUNOENZYMETRIC ASSAY

K Number: K872131 · Decision Aug 25, 1987
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
142
Applicant Total
63
Review Days
82

Basic Information

Device Name
TANDEMR M-PAK LH IMMUNOENZYMETRIC ASSAY
K Number
K872131
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1485
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
HYBRITECH, INC.
Date Received
June 4, 1987
Decision Date
August 25, 1987
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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