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TELEFLEX GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K850677
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1985
Days to Decision
208 days

TELEFLEX GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K850677
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1985
Days to Decision
208 days