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

BIOSIGN HCG I - ONE STEP PREGNANCY TEST

K Number: K981443 · Decision Jun 25, 1998
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
374
Applicant Total
70
Review Days
64

Basic Information

Device Name
BIOSIGN HCG I - ONE STEP PREGNANCY TEST
K Number
K981443
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
PRINCETON BIOMEDITECH CORP.
Date Received
April 22, 1998
Decision Date
June 25, 1998
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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