Last synced on 14 November 2025 at 11:06 pm

LOYON

Page Type
Cleared 510(K)
510(k) Number
K162217
510(k) Type
Traditional
Applicant
Oculus Innovative Sciences
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2017
Days to Decision
227 days
Submission Type
Summary

LOYON

Page Type
Cleared 510(K)
510(k) Number
K162217
510(k) Type
Traditional
Applicant
Oculus Innovative Sciences
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2017
Days to Decision
227 days
Submission Type
Summary