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# GE Healthcare’s Carescape Patient Monitor Cleared
- URL: https://www.fdaweb.com/ge-healthcares-carescape-patient-monitor-cleared/
- Published: 2023-04-20T12:00:00.000Z
- Updated: 2026-09-14T18:26:47.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5154264

FDA has cleared a GE HealthCare 510(k) for its [Carescape Canvas](https://cts.businesswire.com/ct/CT?id=smartlink&url=https%3A%2F%2Fwww.gehealthcare.com%2Fproducts%2Fpatient-monitoring%2Fpatient-monitors%2Fcarescape-canvas&esheet=53384752&newsitemid=20230420005615&lan=en-US&anchor=CARESCAPE+Canvas&index=1&md5=153c93c56f55eda75124da99b5c5697c&ref=fdaweb.com) patient monitoring platform. The company says the Carescape Canvas and its [Carescape ONE](https://cts.businesswire.com/ct/CT?id=smartlink&url=http%3A%2F%2Fwww.gehealthcare.com%2Fproducts%2Fpatient-monitoring%2Fpatient-monitors%2Fcarescape-one&esheet=53384752&newsitemid=20230420005615&lan=en-US&anchor=CARESCAPE+ONE&index=2&md5=27ce98bb360e34fd282a8c7acaba070f&ref=fdaweb.com) are part of an adaptable system that can easily scale up and scale down monitoring capabilities based on the acuity of each individual patient.

“As patient acuity and disease trends change rapidly, adaptability in the hospital setting is becoming more important,” GE says, adding that the device uses the company’s FlexAcutity solution equipped with smart parameter technology that can be tailored to individual patients. It offers “micromodules” that connect with standardized medical USB technology.