Model note · Blood Pressure Monitor
Omron IntelliSense HEM-907XL Professional Blood Pressure Monitor
The HEM-907XL is a professional oscillometric upper arm blood pressure monitor for clinics, examination rooms and bedsides. It inflates automatically, can average several readings, and has a CHECK mode that shows cuff pressure only so the pressure sensor can be compared with a reference manometer. It runs on an AC adapter or rechargeable battery pack and comes with small to extra large cuffs.
The model
Maker, model and type.
- Maker
- Omron Healthcare, Inc.
- Model
- HEM-907XL Professional Blood Pressure Monitor
- Device type
- Blood Pressure Monitor
- Main document
- Open the public document
Key specifications
What the public record says.
| Item | Value | Source |
|---|---|---|
| Method | Oscillometric; capacitive semiconductor pressure sensor; pump inflation, electromagnetic valve deflation and rapid release | Source |
| Measurement range | Pressure 0 to 299 mmHg; pulse 30 to 199 beats/min | Source |
| Accuracy | Pressure within plus or minus 3 mmHg or 2%; pulse within plus or minus 5% of reading | Source |
| Power | AC adapter 120 VAC (13 VA) or battery pack 4.8 VDC, 6 W; auto off after 5 minutes on battery | Source |
| Electrical class and ingress | Class II, type B applied part; IPX0 | Source |
| Operating environment | 10 to 40 C, 30 to 85% RH | Source |
| Size and weight | 139 x 203 x 131 mm; about 910 g | Source |
| Standards | IEC 60601-1, IEC 60601-1-2, AAMI SP10 | Source |
| FDA clearance | K001848, Omron IntelliSense HEM-907, product code DXN, decided 3 July 2000 (510(k) statement) | Source |
Recalls
Recalls.
This note lists no recalls. Check the FDA recall database for the latest record.
Safety
Safety warnings from the record.
- Do not clean with petrol, thinners or strong alcohol, and do not autoclave or gas sterilise the unit. Source
- Unplug the adapter before cleaning and dry the unit fully before reconnecting; it has no ingress protection (IPX0). Source
- After a device error, take the cuff off the patient straight away and remove the unit from service. Source
Sources
Where this note comes from.
- Omron HEM-907XL Instruction Manual (copy on medaval.ie)
- openFDA 510(k) search, HEM-907
- openFDA MAUDE problem counts, model HEM-907XL
Not covered: In the manual's error table the code numbers are printed as display graphics that did not extract; only Er9 is named in the text, so the other entries are labelled by error name and say 'Er series' rather than guessing numbers. The manual copy is hosted by Medaval, not Omron, and its revision date is unknown. No FDA recall names the HEM-907 or HEM-907XL. The K001848 clearance is a 510(k) statement with no public summary.
BMEssentia knowledge drafted from public information, reviewed by Hasan Khaled Ismail on 2026-10-24. Always follow the manufacturer's instructions for use and service manual.
Blood Pressure Monitor
Other models of this device.
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