Class Class II

Aerogen Pro-X1 Controller System (K251615)

K251615 2025-09-02 Traditional
Home/ Devices/ Aerogen Pro-X1 Controller System…

Description

Aerogen Pro-X1 Controller System by Aerogen, Ltd., an FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251615
Clearance Date2025-09-02
Clearance TypeTraditional
Product CodeSFP
Regulation Number868.5630

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top