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

SOMNO STAR & SERIES SLEEP SYSTEM

K Number: K012085 · Decision Aug 2, 2001
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
63
Applicant Total
26
Review Days
30

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Basic Information

Device Name
SOMNO STAR & SERIES SLEEP SYSTEM
K Number
K012085
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sensor Medics Corp.
Date Received
July 3, 2001
Decision Date
August 2, 2001
Product Code
OLV
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
OLV Standard Polysomnograph With Electroencephalograph

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K Number Device Name
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K031883 LYRA NASAL MASK
K030943 MODIFICATION TO HIOX
K022192 PEGASUS NASAL CPAP SYSTEM
K020665 HI-OX
K012034 MODIFICATION TO: SIPAP INFANT NASAL CPAP CIRCUIT
K991972 INFANT FLOW SYSTEM
K984254 INFANT FLOW NCPAP MASKS
K981366 STATIC AND DYNAMIC COMPLIANCE, A RESPIRATORY MECHANICS OPTION FOR THE VMAX SERIES
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