Last synced on 19 July 2024 at 11:05 pm

Model 9160 VitaloQUB

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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