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TrueTear Intranasal Tear Neurostimulator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN170086
510(k) Type
Direct
Applicant
Allergan
Country
United States
FDA Decision
Deleted
Decision Date
5/17/2018
Days to Decision
206 days

TrueTear Intranasal Tear Neurostimulator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN170086
510(k) Type
Direct
Applicant
Allergan
Country
United States
FDA Decision
Deleted
Decision Date
5/17/2018
Days to Decision
206 days