Class Class II

XChange Device, XChange System (K210112)

K210112 2023-01-30 Traditional
Home/ Devices/ XChange Device, XChange System…

Description

XChange Device, XChange System by Pneuma Therapeutics, Inc. — FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK210112
Clearance Date2023-01-30
Clearance TypeTraditional
Product CodeCCK
Regulation Number868.1400

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top