510(k) K222018

Device
Breathe+
Applicant
Peep Medical, LLC Dba Go2 Devices
510(k) number
K222018
Product code
BWF
Decision
Substantially Equivalent (SESE)
Decision date
2023-06-02
Date received
2022-07-08
Regulation
868.5690
Classification name
Spirometer, Therapeutic (Incentive)
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Paul Dryden
Address
9230 Katy Fwy., Suite 600 Houston TX US 77055 77055

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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K163091VibraPEPMedica Holdings, LLC2017-02-21
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