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

DATEX-OHMEDA EEG MODULE, M-EEG AND DATEX-OHMEDA EEG HEADBOX, N-EEG AND ACCESSORIES

K Number: K000892 · Decision Jun 16, 2000
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
53
Applicant Total
58
Review Days
88

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Basic Information

Device Name
DATEX-OHMEDA EEG MODULE, M-EEG AND DATEX-OHMEDA EEG HEADBOX, N-EEG AND ACCESSORIES
K Number
K000892
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Datex-Ohmeda, Inc.
Date Received
March 20, 2000
Decision Date
June 16, 2000
Product Code
OLT
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
OLT Non-Normalizing Quantitative Electroencephalograph Software

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K210384 CARESCAPE R860
K172702 Tec 820, Tec 850
K172045 Aestiva 7900, Aestiva MRI, Aestiva 7100, Aestiva 7100 Compact, Aespire 100, Aespire 7100, Aespire 7900, Aespire View, Avance, Avance CS2, Aisys, Aisys CS2
K170872 Aisys CS2
K151570 Carestation 620/650/650C
K142679 CARESCAPE R860
K143530 Aespire View
K140575 ENGSTROM CARESTATION, ENGSTROM PRO
Search all 58 clearances from Datex-Ohmeda, Inc. →