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QUIKPAC-II ONE STEP PREGNANCY HOME TEST

Page Type
Cleared 510(K)
510(k) Number
K912316
510(k) Type
Traditional
Applicant
SYNTRON BIORESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1991
Days to Decision
61 days
Submission Type
Statement

QUIKPAC-II ONE STEP PREGNANCY HOME TEST

Page Type
Cleared 510(K)
510(k) Number
K912316
510(k) Type
Traditional
Applicant
SYNTRON BIORESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1991
Days to Decision
61 days
Submission Type
Statement