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

Sleepware G3

K Number: K202142 · Decision Oct 29, 2020
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
35
Applicant Total
172
Review Days
90

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Basic Information

Device Name
Sleepware G3
K Number
K202142
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Respironics, Inc.
Date Received
July 31, 2020
Decision Date
October 29, 2020
Product Code
OLZ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
OLZ Automatic Event Detection Software For Polysomnograph With Electroencephalograph

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