Philips Medizin Systeme Boeblingen GmbH

MODIFICATION TO PHILIPS AVALON FETAL MONITORS FM20 AND FM30

All identifiers (2)

Aletia (canonical)ALT-001895

FDA 510(k) · US (primary)K062137

Regulatory Registrations

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FDA

ID: K062137

510k

Last Automated Sync

Mar 2026

Last Clinical Review

Not reviewed

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