Last synced on 29 September 2023 at 11:04 pm

OtoSight Middle Ear Scope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222655
510(k) Type
Special
Applicant
PhotoniCare, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2022
Days to Decision
24 days
Submission Type
Summary

OtoSight Middle Ear Scope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222655
510(k) Type
Special
Applicant
PhotoniCare, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2022
Days to Decision
24 days
Submission Type
Summary