510(k) K191059

Masimo Rad-97 and Accessories by Masimo Corporation — Product Code MWI

K191059 is an FDA 510(k) premarket notification submitted by Masimo Corporation for the device "Masimo Rad-97 and Accessories". The FDA issued a decision of Substantially Equivalent on Dec 27, 2019. The device falls under product code MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)), a Class II device regulated under 21 CFR 870.2300. Masimo Corporation has 86 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Dec 27, 2019
Date Received
Apr 22, 2019
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Device Class
Class II
Regulation Number
870.2300
Review Panel
CV
Submission Type
510(k)