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VENTREX ALLERGEN DISC

Page Type
Cleared 510(K)
510(k) Number
K925044
510(k) Type
Traditional
Applicant
VENTREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/1993
Days to Decision
221 days
Submission Type
Statement

VENTREX ALLERGEN DISC

Page Type
Cleared 510(K)
510(k) Number
K925044
510(k) Type
Traditional
Applicant
VENTREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/1993
Days to Decision
221 days
Submission Type
Statement