VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031)

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K242769 ↗

FDA Product Code

BTL

Models / Variants

VentStar Resus heated (N) (MP17030)

VentStar Autobreath heated (N) (MP17031)

Device Class

Class II

Regulation

21 CFR Part 868.5925

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

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See all devices from Draegerwerk AG & Co. KGaA →