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TERUMO RADIFOCUS INTRODUCER KIT

Page Type
Cleared 510(K)
510(k) Number
K863139
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/1986
Days to Decision
56 days

TERUMO RADIFOCUS INTRODUCER KIT

Page Type
Cleared 510(K)
510(k) Number
K863139
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/1986
Days to Decision
56 days