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SUREFIRE HIGH FLOW ANGIOGRAPHIC CATHETER, ACCESS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122506
510(k) Type
Traditional
Applicant
SUREFIRE MEDICAL, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2012
Days to Decision
31 days
Submission Type
Summary

SUREFIRE HIGH FLOW ANGIOGRAPHIC CATHETER, ACCESS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122506
510(k) Type
Traditional
Applicant
SUREFIRE MEDICAL, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2012
Days to Decision
31 days
Submission Type
Summary