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

VISTA(R) HUMAN CHORIONIC GONADOTROPIN (HCG) ASSAY

K Number: K926342 · Decision Feb 17, 1993
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
374
Applicant Total
448
Review Days
62

Basic Information

Device Name
VISTA(R) HUMAN CHORIONIC GONADOTROPIN (HCG) ASSAY
K Number
K926342
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SYVA CO.
Date Received
December 17, 1992
Decision Date
February 17, 1993
Product Code
JHI
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
JHI Visual, Pregnancy Hcg, Prescription Use

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