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ANGIOPLASTY INJECTOR

Page Type
Cleared 510(K)
510(k) Number
K800613
510(k) Type
Traditional
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/1980
Days to Decision
21 days

ANGIOPLASTY INJECTOR

Page Type
Cleared 510(K)
510(k) Number
K800613
510(k) Type
Traditional
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/1980
Days to Decision
21 days