Last synced on 25 January 2026 at 3:41 am

CLIRPATH TURBO PLUS EXCIMER LASER CATHETERS, MODELS 314-151, 314-159, 317-152, 317-156, 320-006, 320-159, 323-001

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052514
510(k) Type
Traditional
Applicant
Spectranetics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2005
Days to Decision
35 days
Submission Type
Summary

CLIRPATH TURBO PLUS EXCIMER LASER CATHETERS, MODELS 314-151, 314-159, 317-152, 317-156, 320-006, 320-159, 323-001

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052514
510(k) Type
Traditional
Applicant
Spectranetics Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2005
Days to Decision
35 days
Submission Type
Summary