FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

STELLAR 150

K Number: K103167 · Decision Mar 1, 2011
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
24
Applicant Total
8
Review Days
125

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Basic Information

Device Name
STELLAR 150
K Number
K103167
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Resmed Germany, Inc.
Date Received
October 27, 2010
Decision Date
March 1, 2011
Product Code
MNT
Advisory Committee
Anesthesiology
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
MNT Sv70 Ventilator

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K Number Device Name
K143272 ApneaLink Air
K131932 APNEALINK PRO
K122715 STELLAR 150
K113640 STELLAR 150
K083575 APNEALINK PLUS, MODEL: 22328
K070263 APNEALINK
K061405 APNEALINK, MODEL 22302