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

QUICKCARD HCG COMBO TEST, MODEL #9014

K Number: K991095 · Decision Apr 28, 1999
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
47
Review Days
27

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Basic Information

Device Name
QUICKCARD HCG COMBO TEST, MODEL #9014
K Number
K991095
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Phamatech
Date Received
April 1, 1999
Decision Date
April 28, 1999
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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Other Clearances by Phamatech

K Number Device Name
K041578 QUICKSCREEN, MODELS 9177X AND 9178X
K030447 AT HOME DRUG CUP, MODEL 9150X
K010833 AT WORK DRUG TEST, MODEL 9177T AWT
K010836 AT WORK DRUG TEST, MODEL 9147T AWT
K010654 AT HOME DRUG TEST, MODEL 9078 T
K010653 AT HOME DRUG TEST, MODEL 9068 T
K010655 AT HOME DRUG TESTT, MODEL 9150 T
K010645 AT HOME DRUG TEST, MODEL 9063 T
K010646 AT HOME DRUG TEST, MODEL 9083 T
K010651 AT HOME DRUG TEST, MODEL 9133 T
Search all 47 clearances from Phamatech →