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HEARTRAIL III GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K092372
510(k) Type
Traditional
Applicant
TERUMO CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2009
Days to Decision
37 days
Submission Type
Summary

HEARTRAIL III GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K092372
510(k) Type
Traditional
Applicant
TERUMO CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2009
Days to Decision
37 days
Submission Type
Summary