Class Class II

Respiree Cardio-Respiratory Monitor (K223681)

K223681 2023-03-08 Traditional
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Description

Respiree Cardio-Respiratory Monitor by Respiree Pte, Ltd. — FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223681
Clearance Date2023-03-08
Clearance TypeTraditional
Product CodeBZQ
Regulation Number868.2375

Categories

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