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VESSEL DILATOR

Page Type
Cleared 510(K)
510(k) Number
K831190
510(k) Type
Traditional
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1983
Days to Decision
27 days

VESSEL DILATOR

Page Type
Cleared 510(K)
510(k) Number
K831190
510(k) Type
Traditional
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1983
Days to Decision
27 days