(129 days)
Not Found
No
The document describes a standard physiological monitoring module and does not mention any AI or ML capabilities. The focus is on acquiring, processing, and displaying physiological data using established methods.
No.
The "Intended Use / Indications for Use" section explicitly states: "It is not a therapeutic device."
Yes
The device is intended for "monitoring, recording, and alarming of multiple physiological parameters" and provides "processed measurement data (for example, measurement waves and numerics)" for diagnostic purposes, such as "functional oxygen saturation of arterial hemoglobin (SpO2), pulse rate, carboxyhemoglobin saturation (SpCO), methemoglobin saturation (SpMet), total hemoglobin concentration (SpHb), and/or respiratory rate (RRac)". These functions are characteristic of diagnostic devices.
No
The device description explicitly states it is a "Multi-Measurement Module" that "acquires multiple physiological patient signals" and mentions "measurement sensors are applied at diverse body locations." This indicates the device includes hardware components for signal acquisition, not just software.
Based on the provided text, the Philips Multi-Measurement Module (MMX) is not an In Vitro Diagnostic (IVD) device.
Here's why:
- Definition of IVD: In Vitro Diagnostics are medical devices used to perform tests on samples taken from the human body, such as blood, urine, or tissue, to detect diseases, conditions, or infections. These tests are performed outside the body (in vitro).
- Intended Use and Device Description: The text clearly states that the MMX is intended for "monitoring, recording, and alarming of multiple physiological parameters of adults, pediatrics, and neonates." It acquires "physiological patient signals" and uses "measurement sensors are applied at diverse body locations." This describes a device that monitors physiological functions within the body (in vivo) using sensors applied to the patient.
- Lack of Mention of Samples: There is no mention of the device analyzing samples taken from the patient.
- Parameters Measured: The parameters measured (ECG, respiration, SpO2, NBP, invasive pressure, temperature, CO2, SpCO, SpMet, SpHb, RRac) are all physiological parameters measured directly from the patient's body or breath, not from collected samples.
Therefore, the Philips Multi-Measurement Module (MMX) is a patient monitoring device, not an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
The Philips Multi-Measurement Module (MMX) is for use with Philips IntelliVue Patient Monitors.
The Multi-Measurement Module, with its host patient monitor, is intended for monitoring, recording, and alarming of multiple physiological parameters of adults, pediatrics, and neonates in healthcare facilities.
It sends processed measurement data (for example, measurement waves and numerics) to the monitor screen, generates alerts, and supports the transfer of patient data between monitors.
The Multi-Measurement Module is intended for use by trained healthcare professionals in a hospital environment. The Multi-Measurement Module is additionally intended for use in transport situations within hospital environments together with its host patient monitor.
The Multi-Measurement Module is only for use on one patient at a time. It is not intended for home use. It is not a therapeutic device. The Multi-Measurement Module is for prescription use only.
The Masimo rainbow SET measurement is indicated for the noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2), pulse rate, carboxyhemoglobin saturation (SpCO), methemoglobin saturation (SpMet), total hemoglobin concentration (SpHb), and/or respiratory rate (RRac). The Masimo rainbow SET measurement is indicated for use with adult, pediatric, and neonatal patients during both no motion and motion conditions, and for patients who are well or poorly perfused.
Product codes (comma separated list FDA assigned to the subject device)
MHX, DSI, MLD, DSJ, DSK, DXN, DXG, DRQ, DRT, DPS, MLC, DRJ, DQA, DSB, DSA, MSX, CCK, BZO, FLL
Device Description
The newly introduced IntelliVue Multi-Measurement Module MMX acquires multiple physiological patient signals, sends processed measurement data (for example, measurement waves and numerics) to the host monitor screen, generates alerts, and supports the transfer of patient data between monitors.
The device, together with its compatible host monitor, offers a monitoring solution optimized for the surgical, cardiac, medical and neonatal care environments. It can be located in the patient vicinity at the bedside or can be used mobile, during patient transport inside hospitals.
The measurement sensors are applied at diverse body locations, depending on the physiological parameters monitored.
The new device has the same range of functions as the legally marketed predicate devices; it provides the same measurement parameters as the predicates.
The Multi-Measurement Module MMX provides multiple non-invasive and invasive measurements: ECG (including arrhythmia and ST), respiration, SpO2, NBP, dual invasive pressure, temperature, and CO2.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
adults, pediatrics, and neonates
Intended User / Care Setting
trained healthcare professionals in a hospital environment. The Multi-Measurement Module is additionally intended for use in transport situations within hospital environments together with its host patient monitor.
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
The new devices have been subject to a series of V&V activities:
-Testing according to the recognized consensus standards:
- AAMI/ANSI/IEC 62304:2006 (Software life cycle processes)
- AAMI/ANSI ES60601-1:2005/(R)2012 and A1:2012 (Ed. 3.1) (Basic safety and essential performance)
- IEC 60601-1-2:2014 (Ed. 4.0) (Electromagnetic Compatibility)
- IEC 60601-1-8: 2012 (Ed. 2.1) (Alarms)
- IEC 60601-2-25: 2011 (Ed. 2.0) (Electrocardiographs)
- IEC 60601-2-27: 2011 (Ed. 3.0) (ECG monitoring equipment)
- IEC 80601-2-30: 2013 (Ed. 1.1) (Automated noninvasive sphygmomanometers)
- ISO 80601-2-34: 2011 (Ed. 3.0) (Invasive blood pressure monitoring equipment)
- ISO 80601-2-55: 2011 (Ed. 1) (Respiratory gas monitors)
- ISO 80601-2-56: 2009 (Ed. 1) (Clinical thermometers)
- ISO 80601-2-61: 2011 (Ed. 1) (Pulse Oximeters)
All applicable requirements have been met.
-Additional relevant testing according to the device-specific FDA guidance documents:
- "Pulse Oximeters Premarket Notification Submissions [510(k)s] -Guidance for Industry and Food and Drug Administration Staff"
- Accuracy of Pulse Oximeters
- Testing that demonstrates that SpO₂ and pulse rate values calculated by the OEM system are not corrupted during communication to the host device
- Display values, outputs, and indicators.
All applicable requirements have been met.
- "Non-Invasive Blood Pressure (NBP) Monitor Guidance"
- The intra-device variability between a minimum of three devices
- Comparison to the intra-arterial reference standard for mean blood pressure.
All applicable requirements have been met.
-Testing as required by the Hazard Analysis
All specified pass/fail criteria have been met. The test results have confirmed the effectiveness of the implemented design risk mitigation measures.
-Additional environmental testing (temperature, humidity) and mechanical testing (mechanical classes 7M1, 7M2, 7M3)
All specified test requirements have been met. The tests have confirmed that the new devices work safely and according to their specifications and indicated claims during tests simulating general hospital conditions, handling and transport in hospital environments and storage.
-Integration tests, functional system level tests, and regression system level tests
The new devices perform according to the specified criteria:
- Integration tests
- Functional tests for physiological parameters
- Regression tests for patient monitor compatibility and operating system
All specified test requirements have been met. The test results demonstrate that modified and previously available device functions work correctly according to the specifications and labeling claims.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 870.1025 Arrhythmia detector and alarm (including ST-segment measurement and alarm).
(a)
Identification. The arrhythmia detector and alarm device monitors an electrocardiogram and is designed to produce a visible or audible signal or alarm when atrial or ventricular arrhythmia, such as premature contraction or ventricular fibrillation, occurs.(b)
Classification. Class II (special controls). The guidance document entitled “Class II Special Controls Guidance Document: Arrhythmia Detector and Alarm” will serve as the special control. See § 870.1 for the availability of this guidance document.
0
Image /page/0/Picture/0 description: The image contains the logo for the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.
November 15, 2018
Philips Medizin Systeme Boeblingen GmbH Stefan Breuer Senior Regulatory Affairs Engineer Hewlett-Packard-Str. 2 Boeblingen, 71034 De
Re: K181831
Trade/Device Name: IntelliVue Multi-Measurement Module MMX Regulation Number: 21 CFR 870.1025 Regulation Name: Arrhythmia Detector and Alarm (Including ST-Segment Measurement and Alarm) Regulatory Class: Class II Product Code: MHX, DSI, MLD, DSJ, DSK, DXN, DXG, DRQ, DRT, DPS, MLC, DRJ, DQA, DSB, DSA, MSX, CCK, BZO, FLL Dated: October 11, 2018 Received: October 15, 2018
Dear Stefan Breuer:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You mav, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be avare that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's
1
requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/CombinationProducts/GuidanceRegulatoryInformation/ucm597488.html; good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm.
For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/) and CDRH Learn (http://www.fda.gov/Training/CDRHLearn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (http://www.fda.gov/DICE) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely.
Arielle Drummond -S
For
Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
2
DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration
Indications for Use
510(k) Number (if known) K181831
Device Name IntelliVue Multi-Measurement Module MMX
Indications for Use (Describe)
The Philips Multi-Measurement Module (MMX) is for use with Philips IntelliVue Patient Monitors.
The Multi-Measurement Module, with its host patient monitor, is intended for monitoring, recording, and alarming of multiple physiological parameters of adults, pediatrics, and neonates in healthcare facilities.
It sends processed measurement data (for example, measurement waves and numerics) to the monitor screen, generates alerts, and supports the transfer of patient data between monitors.
The Multi-Measurement Module is intended for use by trained healthcare professionals in a hospital environment. The Multi-Measurement Module is additionally intended for use in transport situations within hospital environments together with its host patient monitor.
The Multi-Measurement Module is only for use on one patient at a time. It is not intended for home use. It is not a therapeutic device. The Multi-Measurement Module is for prescription use only.
The Masimo rainbow SET measurement is indicated for the nonitoring of functional oxygen saturation of arterial hemoglobin (SpO2), pulse rate, carboxyhemoglobin saturation (SpCO), methemoglobin saturation (SpMet), total hemoglobin concentration (SpHb), and/or respiratory rate (RRac). The Masimo rainbow SET measurement is indicated for use with adult, pediatric, and neonatal patients during both no motion conditions, and for patients who are well or poorly perfused.
| Type of Use (Select one or both, as applicable) | ☑ Prescription Use (Part 21 CFR 801 Subpart D) ☐ Over-The-Counter Use (21 CFR 801 Subpart C) |
|---|---|
| ------------------------------------------------- | ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ |
CONTINUE ON A SEPARATE PAGE IF NEEDED
This section applies only to requirements of the Paperwork Reduction Act of 1995.
DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.
The burden time for this collection of information is estimated to average 79 hours per response, including the time to
review instructions, search existing data sources, gather and maintain the data needed and complete and review the
collection of information. Send comments regarding this burden estimate or any other aspect of this information
collection, including suggestions for reducing this burden, to:
Department of Health and Human Services
Food and Drug Administration
Office of Chief Information Officer
Paperwork Reduction Act (PRA) Staff
"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of
information unless it displays a currently valid OMB number."
FORM EDA 3881 (7/17)
Page 1 of 1
PSC Publishing Services (301) 443 6740
EE
FORM FDA 3881 (7/17) Page 1 of 1 PSC Publishing Services (301) 443-6740 EF
3
510(k) Summary
This summary of 510(k) safety and effectiveness information is submitted in accordance with the requirements of the Safe Medical Devices Act of 1990 and 21 C.F.R. §807.92.
5.1 Submitter
The submitter of this Premarket Notification is:
Stefan Breuer Philips Medizin Systeme Boeblingen GmbH Hewlett-Packard-Str. 2 71034 Boeblingen Germany Telephone: +49 7031 463-2321 +49 7031 463-2442 Fax: Email: stefan.breuer@philips.com This summary was prepared on July 04, 2018.
5.2 Name and Classification of the Devices
Trade names: IntelliVue Multi-Measurement Module MMX Common name: Multifunction Patient Monitor Module
Classification:
| Device Panel | Classification | ProCode | Description |
|---|---|---|---|
| Cardiovascular | |||
| Devices | §870.1025, II | MHX | Monitor, Physiological, Patient (with |
| arrhythmia detection or alarms) | |||
| Cardiovascular | |||
| Devices | §870.1025, II | DSI | Detector and alarm, arrhythmia |
| Cardiovascular | |||
| Devices | §870.1025, II | MLD | Monitor, ST Segment with Alarm |
| Cardiovascular | |||
| Devices | §870.1100, II | DSJ | Alarm, Blood Pressure |
| Cardiovascular | |||
| Devices | §870.1110, II | DSK | Computer, Blood Pressure |
| Cardiovascular | |||
| Devices | §870.1130, II | DXN | System, Measurement, Blood- |
| Pressure, Non-Invasive | |||
| Cardiovascular | |||
| Devices | §870.1435, II | DXG | Computer, Diagnostic, Pre- |
| Programmed, Single-Function | |||
| Cardiovascular | |||
| Devices | §870.2060, II | DRQ | Amplifier and Signal Conditioner, |
| Transducer Signal | |||
| Cardiovascular | |||
| Devices | §870.2300, II | DRT | Monitor, Cardiac (incl. |
| Cardiotachometer & Rate Alarm) | |||
| Cardiovascular | |||
| Devices | §870.2340, II | DPS | Electrocardiograph |
| Cardiovascular | |||
| Devices | §870.2340, II | MLC | Monitor, ST Segment |
| Cardiovascular | |||
| Devices | §870.2600, I | DRJ | System, Signal Isolation |
| Cardiovascular | |||
| Devices | §870.2700, II | DQA | Oximeter |
| Cardiovascular | |||
| Devices | §870.2770, II | DSB | Plethysmograph, Impedance |
| Cardiovascular | |||
| Devices | §870.2900, I | DSA | Cable, Transducer and Electrode, |
| incl. Patient Connector | |||
| - | MSX | System, Network and | |
| Communication, Physiological | |||
| Monitors |
4
| Device Panel | Classification | ProCode | Description |
|---|---|---|---|
| Anesthesiology | |||
| Devices | §868.1400, II | CCK | Analyzer, Gas, Carbon Dioxide, |
| Gaseous-Phase | |||
| §868.2375, II | BZQ | Monitor, Breathing Frequency | |
| General Hospital and | |||
| Personal Use | |||
| Devices | §880.2910, II | FLL | Thermometer, Electronic, Clinical |
5.3 Substantial Equivalence
The newly introduced IntelliVue Multi-Measurement Module MMX is substantially equivalent to
- . the legally marketed IntelliVue Multi-Measurement Module X1 with Capnography Extension M3014A, marketed pursuant to K161531 and K050762
- the legally marketed IntelliVue Multi-Measurement Module X3, marketed pursuant ● to K171801.
5.4 Description of the Device
The newly introduced IntelliVue Multi-Measurement Module MMX acquires multiple physiological patient signals, sends processed measurement data (for example, measurement waves and numerics) to the host monitor screen, generates alerts, and supports the transfer of patient data between monitors.
The device, together with its compatible host monitor, offers a monitoring solution optimized for the surgical, cardiac, medical and neonatal care environments. It can be located in the patient vicinity at the bedside or can be used mobile, during patient transport inside hospitals.
The measurement sensors are applied at diverse body locations, depending on the physiological parameters monitored.
The new device has the same range of functions as the legally marketed predicate devices; it provides the same measurement parameters as the predicates.
The Multi-Measurement Module MMX provides multiple non-invasive and invasive measurements: ECG (including arrhythmia and ST), respiration, SpO2, NBP, dual invasive pressure, temperature, and CO2.
5.5 Intended Use
The Philips Multi-Measurement Module MMX is for use with Philips IntelliVue Patient Monitors.
The Multi-Measurement Module, with its host patient monitor, is intended for monitoring, recording, and alarming of multiple physiological parameters of adults, pediatrics, and neonates in health care facilities.
It sends processed measurement data (for example, measurement waves and numerics) to the monitor screen, generates alerts, and supports the transfer of patient data between monitors.
5
The Multi-Measurement Module is intended for use by trained healthcare professionals in a hospital environment. The Multi-Measurement Module is additionally intended for use in transport situations within hospital environments together with its host patient monitor.
The Multi-Measurement Module is only for use on one patient at a time. It is not intended for home use. It is not a therapeutic device. The Multi-Measurement Module is for prescription use only.
The Masimo rainbow SET measurement is indicated for the noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2), pulse rate, carboxyhemoglobin saturation (SpCO), methemoglobin saturation (SpMet), total hemoglobin concentration (SpHb), and/or respiratory rate (RRac). The Masimo rainbow SET measurement is indicated for use with adult, pediatric, and neonatal patients during both no motion and motion conditions, and for patients who are well or poorly perfused.
5.6 Technological Characteristics
The new IntelliVue Multi-Measurement Module MMX has the same technological characteristics as its predicate device IntelliVue Multi-Measurement Module X1 with Capnography Extension M3014A. It has the same operating principles, mechanism of action, energy sources, portability, user interface, and comparable robustness. Dimensions, weight and environmental specifications are very similar.
The new IntelliVue Multi-Measurement Module MMX also has the same technological characteristics as its predicate device IntelliVue Multi-Measurement Module X3. It has the same operating principles, mechanism of action, portability and robustness. The implementation of the physiological measurements are identical in hardware and software. Dimensions, weight and environmental specifications are very similar.
5.7 Summary of V&V Activities
The new devices have been subject to a series of V&V activities:
- Testing according to the recognized consensus standards: ●
- o AAMI/ANSI/IEC 62304:2006 (Software life cycle processes)
- o AAMI/ANSI ES60601-1:2005/(R)2012 and A1:2012 (Ed. 3.1) (Basic safety and essential performance)
- IEC 60601-1-2:2014 (Ed. 4.0) (Electromagnetic Compatibility) O
- IEC 60601-1-8: 2012 (Ed. 2.1) (Alarms) O
- IEC 60601-2-25: 2011 (Ed. 2.0) (Electrocardiographs) O
- IEC 60601-2-27: 2011 (Ed. 3.0) (ECG monitoring equipment) O
- IEC 80601-2-30: 2013 (Ed. 1.1) (Automated noninvasive O sphygmomanometers)
- O IEC 60601-2-34: 2011 (Ed. 3.0) (Invasive blood pressure monitoring equipment)
- ISO 80601-2-55: 2011 (Ed. 1) (Respiratory gas monitors) O
- ISO 80601-2-56: 2009 (Ed. 1) (Clinical thermometers) O
- ISO 80601-2-61: 2011 (Ed. 1) (Pulse Oximeters) O
6
All applicable requirements have been met.
- Additional relevant testing according to the device-specific FDA guidance ● documents:
- o "Pulse Oximeters Premarket Notification Submissions [510(k)s] -Guidance for Industry and Food and Drug Administration Staff"
- Accuracy of Pulse Oximeters ■
- Testing that demonstrates that SpO₂ and pulse rate values calculated . by the OEM system are not corrupted during communication to the host device
- . Display values, outputs, and indicators.
- All applicable requirements have been met.
- "Non-Invasive Blood Pressure (NBP) Monitor Guidance" O
- The intra-device variability between a minimum of three devices
- . Comparison to the intra-arterial reference standard for mean blood pressure.
- o "Pulse Oximeters Premarket Notification Submissions [510(k)s] -Guidance for Industry and Food and Drug Administration Staff"
All applicable requirements have been met.
- Testing as required by the Hazard Analysis ● All specified pass/fail criteria have been met. The test results have confirmed the effectiveness of the implemented design risk mitigation measures.
- Additional environmental testing (temperature, humidity) and mechanical testing ● (mechanical classes 7M1, 7M2, 7M3) All specified test requirements have been met. The tests have confirmed that the new devices work safely and according to their specifications and indicated claims during tests simulating general hospital conditions, handling and transport in hospital environments and storage.
- Integration tests, functional system level tests, and regression system level tests ● The new devices perform according to the specified criteria:
- o Integration tests
- o Functional tests for physiological parameters
Regression tests for patient monitor compatibility and operating system o All specified test requirements have been met. The test results demonstrate that modified and previously available device functions work correctly according to the specifications and labeling claims.
5.8 Conclusion
Verification, validation, and testing activities establish the performance, functionality, and reliability characteristics of the new device with respect to the predicates.
Testing comprised electrical and mechanical safety tests, EMC tests, environmental tests, performance tests, functional and regression tests.
Pass/Fail criteria were based on the specifications cleared for the predicate devices and test results showed substantial equivalence.
The results demonstrate that the new devices meet all defined reliability requirements and performance claims.