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VENTREX COATED TUBE HCG

Page Type
Cleared 510(K)
510(k) Number
K890549
510(k) Type
Traditional
Applicant
VENTREX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1989
Days to Decision
53 days

VENTREX COATED TUBE HCG

Page Type
Cleared 510(K)
510(k) Number
K890549
510(k) Type
Traditional
Applicant
VENTREX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1989
Days to Decision
53 days