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10 AND 12 FRENCH VESSEL DILATORS

Page Type
Cleared 510(K)
510(k) Number
K874738
510(k) Type
Traditional
Applicant
IMPRA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1988
Days to Decision
166 days

10 AND 12 FRENCH VESSEL DILATORS

Page Type
Cleared 510(K)
510(k) Number
K874738
510(k) Type
Traditional
Applicant
IMPRA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1988
Days to Decision
166 days