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SET, INTRAVASCULAR

Page Type
Cleared 510(K)
510(k) Number
K881975
510(k) Type
Traditional
Applicant
PRIMROSE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/1988
Days to Decision
79 days

SET, INTRAVASCULAR

Page Type
Cleared 510(K)
510(k) Number
K881975
510(k) Type
Traditional
Applicant
PRIMROSE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/1988
Days to Decision
79 days