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TORQUE DEVICE FOR A GUIDE WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910969
510(k) Type
Traditional
Applicant
TERUMO CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/1991
Days to Decision
71 days

TORQUE DEVICE FOR A GUIDE WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910969
510(k) Type
Traditional
Applicant
TERUMO CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/1991
Days to Decision
71 days