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

TESTPACK PLUS HCG URINE

K Number: K954029 · Decision Oct 5, 1995
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
883
Review Days
38

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Basic Information

Device Name
TESTPACK PLUS HCG URINE
K Number
K954029
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Laboratories
Date Received
August 28, 1995
Decision Date
October 5, 1995
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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