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MEDRAD OPEN ENDED GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K880332
510(k) Type
Traditional
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1988
Days to Decision
184 days

MEDRAD OPEN ENDED GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K880332
510(k) Type
Traditional
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1988
Days to Decision
184 days