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RADIFOCUS(R) (CATHETER) GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K924202
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1992
Days to Decision
95 days
Submission Type
Summary

RADIFOCUS(R) (CATHETER) GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K924202
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1992
Days to Decision
95 days
Submission Type
Summary