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RADIFOCUS GLIDEWIRE FOR CORONARY USE WITH PLATINUM (OR GOLD) COIL

Page Type
Cleared 510(K)
510(k) Number
K953533
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1995
Days to Decision
83 days
Submission Type
Summary

RADIFOCUS GLIDEWIRE FOR CORONARY USE WITH PLATINUM (OR GOLD) COIL

Page Type
Cleared 510(K)
510(k) Number
K953533
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1995
Days to Decision
83 days
Submission Type
Summary