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OPTOSSOL COMPRESSION DEVICE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K140875
510(k) Type
Traditional
Applicant
GENOSSIS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2014
Days to Decision
56 days
Submission Type
Summary

OPTOSSOL COMPRESSION DEVICE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K140875
510(k) Type
Traditional
Applicant
GENOSSIS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2014
Days to Decision
56 days
Submission Type
Summary