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QUIKPAC II, ONE STEP HCG COMBO KIT

Page Type
Cleared 510(K)
510(k) Number
K945951
510(k) Type
Traditional
Applicant
SYNTRON BIORESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1995
Days to Decision
64 days
Submission Type
Summary

QUIKPAC II, ONE STEP HCG COMBO KIT

Page Type
Cleared 510(K)
510(k) Number
K945951
510(k) Type
Traditional
Applicant
SYNTRON BIORESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1995
Days to Decision
64 days
Submission Type
Summary