Class Class II

Breathe+ (K222018)

K222018 2023-06-02 Traditional
Home/ Devices/ Breathe+ (K222018)

Description

Breathe+ by Peep Medical, LLC Dba Go2 Devices — FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222018
Clearance Date2023-06-02
Clearance TypeTraditional
Product CodeBWF
Regulation Number868.5690

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top