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IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230604
510(k) Type
Traditional
Applicant
Philips Medizin Systeme Boeblingen GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/22/2023
Days to Decision
264 days
Submission Type
Summary

IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230604
510(k) Type
Traditional
Applicant
Philips Medizin Systeme Boeblingen GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
11/22/2023
Days to Decision
264 days
Submission Type
Summary