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

CRYSTAL-EEG MODEL 10 (MODEL 10)

K Number: K970672 · Decision May 22, 1997
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
27
Applicant Total
8
Review Days
87

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Basic Information

Device Name
CRYSTAL-EEG MODEL 10 (MODEL 10)
K Number
K970672
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
February 24, 1997
Decision Date
May 22, 1997
Product Code
OMC
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
OMC Reduced- Montage Standard Electroencephalograph

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OMC), ordered by most recent decision date.

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Other Clearances by Cleveland Medical Devices, Inc.

K Number Device Name
K063872 KINESIA
K042039 FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120
K013863 CRYSTAL MONITOR MODEL 16
K001110 CRYSTAL-EEG MODEL 15
K964690 LIBERTY VALVE
K962591 FOOT WEIGHT ALARM
K954670 PRESSORE MONITOR