ORi— 510(k) DEN200076

Unknown

Masimo Corporation

FDA 510(k) clearance DEN200076 for ORi, Unknown on 2023-10-12. Applicant: Masimo Corporation. Device class: 2.

Clearance details

Applicant: Masimo Corporation
Product code: Code QWE
Device class: Class 2
Regulation: 21 CFR 870.2720
Advisory panel: Anesthesiology
Date received: 2020-12-21
Decision date: 2023-10-12
Decision: Unknown
Clearance type: Direct
Location: Irvine, CA, US

View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.