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

WUNDER PREGNANCY TEST

K Number: K130456 · Decision Apr 8, 2014
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
1
Review Days
410

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Basic Information

Device Name
WUNDER PREGNANCY TEST
K Number
K130456
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
James Nguyen
Date Received
February 22, 2013
Decision Date
April 8, 2014
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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