Last synced on 25 January 2026 at 3:41 am

Model 9160 VitaloQUB

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223818
510(k) Type
Traditional
Applicant
Vitalograph Ireland, Ltd.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
5/25/2023
Days to Decision
155 days
Submission Type
Summary

Model 9160 VitaloQUB

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223818
510(k) Type
Traditional
Applicant
Vitalograph Ireland, Ltd.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
5/25/2023
Days to Decision
155 days
Submission Type
Summary