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TRIO Handpiece

Page Type
Cleared 510(K)
510(k) Number
K183199
510(k) Type
Traditional
Applicant
OmniGuide, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2019
Days to Decision
164 days
Submission Type
Summary

TRIO Handpiece

Page Type
Cleared 510(K)
510(k) Number
K183199
510(k) Type
Traditional
Applicant
OmniGuide, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2019
Days to Decision
164 days
Submission Type
Summary