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OCELOT CATHETER

Page Type
Cleared 510(K)
510(k) Number
K123462
510(k) Type
Special
Applicant
AVINGER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2012
Days to Decision
28 days
Submission Type
Summary

OCELOT CATHETER

Page Type
Cleared 510(K)
510(k) Number
K123462
510(k) Type
Special
Applicant
AVINGER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2012
Days to Decision
28 days
Submission Type
Summary