IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036)
K-Number: K252726 · 2026-02-06
Device Summary
Frequently Asked Questions
What is the IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036)?
IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036) is a medical device that received FDA 510(k) clearance on 2026-02-06. It is manufactured by Philips Medizin Systeme Boeblingen GmbH. The 510(k) number is K252726.
When was IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036) approved by the FDA?
IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036) received FDA 510(k) clearance on 2026-02-06, under approval number K252726.
What company makes IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036)?
IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036) is manufactured by Philips Medizin Systeme Boeblingen GmbH.
What is the FDA product code for IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036)?
The FDA product code for IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036) is MHX.
Related Clinical Trials
Related PubMed Literature
Other Devices by Philips Medizin Systeme Boeblingen GmbH
Related Devices (Code: MHX)
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.