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

Radical-7 Pulse CO-Oximeter and Accessories, Rad-97 and Accessories

K Number: K212161 · Decision Mar 6, 2023
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
305
Applicant Total
85
Review Days
602

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Basic Information

Device Name
Radical-7 Pulse CO-Oximeter and Accessories, Rad-97 and Accessories
K Number
K212161
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Masimo Corporation
Date Received
July 12, 2021
Decision Date
March 6, 2023
Product Code
MWI
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

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