Class Class II

PrevisEA Device (K230769)

K230769 2023-05-19 Traditional
Home/ Devices/ PrevisEA Device (K230769)

Description

PrevisEA Device by Entac Medical, Inc. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230769
Clearance Date2023-05-19
Clearance TypeTraditional
Product CodeDQD
Regulation Number870.1875

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top