Oximax Neomax Adhesive Forehead Reflectance Oximetry Sensor

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K051271 ↗

FDA Product Code

DQA

Device Class

Class II

Regulation

21 CFR Part 870.2700

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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See all devices from Nellcor Puritan Bennett, Inc. →