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

FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120

K Number: K042039 · Decision Nov 17, 2004
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
63
Applicant Total
8
Review Days
111

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Basic Information

Device Name
FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120
K Number
K042039
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cleveland Medical Devices, Inc.
Date Received
July 29, 2004
Decision Date
November 17, 2004
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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Other Clearances by Cleveland Medical Devices, Inc.

K Number Device Name
K063872 KINESIA
K013863 CRYSTAL MONITOR MODEL 16
K001110 CRYSTAL-EEG MODEL 15
K970672 CRYSTAL-EEG MODEL 10 (MODEL 10)
K964690 LIBERTY VALVE
K962591 FOOT WEIGHT ALARM
K954670 PRESSORE MONITOR