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BRIDGEPOINT MEDICAL ENTERA PERCUTANEOUS CORONARY AND PERIPHERAL GUIDEWIRE, MODEL M-3001

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081187
510(k) Type
Traditional
Applicant
BRIDGEPOINT MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2008
Days to Decision
163 days
Submission Type
Summary

BRIDGEPOINT MEDICAL ENTERA PERCUTANEOUS CORONARY AND PERIPHERAL GUIDEWIRE, MODEL M-3001

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081187
510(k) Type
Traditional
Applicant
BRIDGEPOINT MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2008
Days to Decision
163 days
Submission Type
Summary