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FDA 510(k)

Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System

K-Number: K203208 · 2022-06-12

Decision Date2022-06-12
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System is a medical device manufactured by Taiwan Aulisa Medical Devices Technologies, Inc.. It received FDA 510(k) clearance on 2022-06-12 under approval number K203208. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System?

Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System is a medical device that received FDA 510(k) clearance on 2022-06-12. It is manufactured by Taiwan Aulisa Medical Devices Technologies, Inc.. The 510(k) number is K203208.

When was Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System approved by the FDA?

Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System received FDA 510(k) clearance on 2022-06-12, under approval number K203208.

What company makes Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System?

Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System is manufactured by Taiwan Aulisa Medical Devices Technologies, Inc..

What is the FDA product code for Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System?

The FDA product code for Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System is DQA.

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Official Source

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