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CATHETER, INTRAVASCULAR

Page Type
Cleared 510(K)
510(k) Number
K881976
510(k) Type
Traditional
Applicant
PRIMROSE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1988
Days to Decision
85 days

CATHETER, INTRAVASCULAR

Page Type
Cleared 510(K)
510(k) Number
K881976
510(k) Type
Traditional
Applicant
PRIMROSE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1988
Days to Decision
85 days