Last synced on 14 November 2025 at 11:06 pm

MODIFIED VENTRESCREEN BETA HCG ENZYME IMMUNOASSAY

Page Type
Cleared 510(K)
510(k) Number
K880678
510(k) Type
Traditional
Applicant
VENTREX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1988
Days to Decision
46 days

MODIFIED VENTRESCREEN BETA HCG ENZYME IMMUNOASSAY

Page Type
Cleared 510(K)
510(k) Number
K880678
510(k) Type
Traditional
Applicant
VENTREX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1988
Days to Decision
46 days