IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030)
K-Number: K230604 · 2023-11-22
Device Summary
Frequently Asked Questions
What is the IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030)?
IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030) is a medical device that received FDA 510(k) clearance on 2023-11-22. It is manufactured by Philips Medizin Systeme Boeblingen GmbH. The 510(k) number is K230604.
When was IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030) approved by the FDA?
IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030) received FDA 510(k) clearance on 2023-11-22, under approval number K230604.
What company makes IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030)?
IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030) is manufactured by Philips Medizin Systeme Boeblingen GmbH.
What is the FDA product code for IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030)?
The FDA product code for IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030) is MHX.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.