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VENTREX ALLERGEN DISC

Page Type
Cleared 510(K)
510(k) Number
K913833
510(k) Type
Traditional
Applicant
VENTREX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1992
Days to Decision
179 days
Submission Type
Statement

VENTREX ALLERGEN DISC

Page Type
Cleared 510(K)
510(k) Number
K913833
510(k) Type
Traditional
Applicant
VENTREX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/1992
Days to Decision
179 days
Submission Type
Statement