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RSI FEMORAL GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K902943
510(k) Type
Traditional
Applicant
RETROPERFUSION SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/1990
Days to Decision
90 days

RSI FEMORAL GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K902943
510(k) Type
Traditional
Applicant
RETROPERFUSION SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/1990
Days to Decision
90 days