Last synced on 25 April 2025 at 11:05 pm

IntelliVue Patient Monitor MX400 (866060), IntelliVue Patient Monitor MX450 (866062), IntelliVue Patient Monitor MX500 (866064), IntelliVue Patient Monitor MX550 (866066)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223574
510(k) Type
Traditional
Applicant
Philips Medizin Systeme Boeblingen GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/22/2023
Days to Decision
265 days
Submission Type
Summary

IntelliVue Patient Monitor MX400 (866060), IntelliVue Patient Monitor MX450 (866062), IntelliVue Patient Monitor MX500 (866064), IntelliVue Patient Monitor MX550 (866066)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223574
510(k) Type
Traditional
Applicant
Philips Medizin Systeme Boeblingen GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/22/2023
Days to Decision
265 days
Submission Type
Summary