Class Class II

Passeo-35 Xeo Peripheral Dilatation Catheter (K222065)

K222065 2023-02-16 Traditional
Home/ Devices/ Passeo-35 Xeo Peripheral Dilatation…

Description

Passeo-35 Xeo Peripheral Dilatation Catheter by Biotronik, Inc. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222065
Clearance Date2023-02-16
Clearance TypeTraditional
Product CodeLIT
Regulation Number870.1250

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top