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RADIFOCUS INTRODUCER II KIT

Page Type
Cleared 510(K)
510(k) Number
K954234
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1995
Days to Decision
77 days
Submission Type
Summary

RADIFOCUS INTRODUCER II KIT

Page Type
Cleared 510(K)
510(k) Number
K954234
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1995
Days to Decision
77 days
Submission Type
Summary