Class Class II

Bloomlife MFM-Pro (K222327)

K222327 2023-02-13 Traditional
Home/ Devices/ Bloomlife MFM-Pro (K222327)

Description

Bloomlife MFM-Pro by Bloom Technologies NV — FDA 510(k) cleared obstetrics/gynecology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222327
Clearance Date2023-02-13
Clearance TypeTraditional
Product CodeHGM
Regulation Number884.2740

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top