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INTRODUCER, PERCUTANEOUS

Page Type
Cleared 510(K)
510(k) Number
K870907
510(k) Type
Traditional
Applicant
MEDFUSION SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1987
Days to Decision
35 days

INTRODUCER, PERCUTANEOUS

Page Type
Cleared 510(K)
510(k) Number
K870907
510(k) Type
Traditional
Applicant
MEDFUSION SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1987
Days to Decision
35 days