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OCELOT CATHETER, OCELOT PIXL CATHETER, LIGHTBOX CONSOLE

Page Type
Cleared 510(K)
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)
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