FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

Disposable BreathSensor Adult, Disposable BreathSensor Small Adult / Child, Disposable BreathSensor Preemie, Disposable BreathSensor Infant

K Number: K180001 · Decision Sep 27, 2019
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
160
Applicant Total
8
Review Days
633

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Basic Information

Device Name
Disposable BreathSensor Adult, Disposable BreathSensor Small Adult / Child, Disposable BreathSensor Preemie, Disposable BreathSensor Infant
K Number
K180001
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Embla Systems
Date Received
January 2, 2018
Decision Date
September 27, 2019
Product Code
MNR
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
MNR Ventilatory Effort Recorder

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