CELLAVISION DM1200 WITH THE BODY FLUID APPLICTION

CellaVision AB · Manufacturer

All identifiers (2)

Aletia (canonical)ALT-002358

FDA 510(k) · US (primary)K102778

Regulatory Registrations

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FDA

ID: K102778

510k

Last Automated Sync

Mar 2026

Last Clinical Review

Not reviewed

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