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OCELOT CATHETER, OCELOT PIXL CATHETER, LIGHTBOX CONSOLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140185
510(k) Type
Traditional
Applicant
Avinger, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2014
Days to Decision
97 days
Submission Type
Summary

OCELOT CATHETER, OCELOT PIXL CATHETER, LIGHTBOX CONSOLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140185
510(k) Type
Traditional
Applicant
Avinger, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2014
Days to Decision
97 days
Submission Type
Summary