FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Masimo W1

K Number: K243305 · Decision Apr 3, 2025
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
85
Review Days
164

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Basic Information

Device Name
Masimo W1
K Number
K243305
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Masimo Corporation
Date Received
October 21, 2024
Decision Date
April 3, 2025
Product Code
DPS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DPS Electrocardiograph

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K232512 Masimo W1
DEN200076 ORi
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