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MINI TREK(TM) RX AND TREK(TM) RX CORONARY DILATATION CATHETER MINI TREK(TM) OTW AND TREK(TM) OTW DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103110
510(k) Type
Traditional
Applicant
ABBOTT VASCULAR-CARDIAC THERAPIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2011
Days to Decision
94 days
Submission Type
Summary

MINI TREK(TM) RX AND TREK(TM) RX CORONARY DILATATION CATHETER MINI TREK(TM) OTW AND TREK(TM) OTW DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103110
510(k) Type
Traditional
Applicant
ABBOTT VASCULAR-CARDIAC THERAPIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2011
Days to Decision
94 days
Submission Type
Summary