510(k) K250934

Device
Respiree Cardio- Respiratory Monitor System
Applicant
Respiree Pte, Ltd.
510(k) number
K250934
Product code
BZQ
Decision
Substantially Equivalent (SESE)
Decision date
2025-08-05
Date received
2025-03-28
Regulation
868.2375
Classification name
Monitor, Breathing Frequency
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Samantha Chow
Address
176 Orchard Rd., #05-05 The Centrepoint Singapore Central SG 238843 238843

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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