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CATHETER, INTRAVASCULAR OR PERCUTANEOUS

Page Type
Cleared 510(K)
510(k) Number
K951078
510(k) Type
Traditional
Applicant
SIMS DELTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1995
Days to Decision
144 days
Submission Type
Summary

CATHETER, INTRAVASCULAR OR PERCUTANEOUS

Page Type
Cleared 510(K)
510(k) Number
K951078
510(k) Type
Traditional
Applicant
SIMS DELTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1995
Days to Decision
144 days
Submission Type
Summary