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QUICKCARD PRO HCG TEST, MODEL 9008

Page Type
Cleared 510(K)
510(k) Number
K980896
510(k) Type
Traditional
Applicant
PHAMATECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1998
Days to Decision
24 days
Submission Type
Summary

QUICKCARD PRO HCG TEST, MODEL 9008

Page Type
Cleared 510(K)
510(k) Number
K980896
510(k) Type
Traditional
Applicant
PHAMATECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1998
Days to Decision
24 days
Submission Type
Summary