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RADIUS PTCA GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K970466
510(k) Type
Traditional
Applicant
RADIUS MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1997
Days to Decision
102 days
Submission Type
Summary

RADIUS PTCA GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K970466
510(k) Type
Traditional
Applicant
RADIUS MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1997
Days to Decision
102 days
Submission Type
Summary