Nellcor Indgo Manual Resuscitator

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K023494 ↗

FDA Product Code

BTM

Device Class

Class II

Regulation

21 CFR Part 868.5915

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

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See all devices from Nellcor Puritan Bennett, Inc. →