Optovent AB

OPTOVENT RESPONS, OPTOVENT RENEE (OPTOVENT RESPONS WITHOUT PULSE OXIMETRY MODULE)

All identifiers (2)

Aletia (canonical)ALT-001291

FDA 510(k) · US (primary)K003704

Regulatory Registrations

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FDA

ID: K003704

510k

Last Automated Sync

Mar 2026

Last Clinical Review

Not reviewed

This listing was auto-populated from public registry data

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