510(k) K243305

Device
Masimo W1
Applicant
Masimo Corporation
510(k) number
K243305
Product code
DPS
Decision
Substantially Equivalent (SESE)
Decision date
2025-04-03
Date received
2024-10-21
Regulation
870.2340
Classification name
Electrocardiograph
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Sindura Penubarthi
Address
52 Discovery Irvine CA US 92618 92618

FDA Registration Numbers

Source Documents

510(k) summary PDF

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