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

SPACELABS MODEL 90480 EEG MODULE

K Number: K896942 · Decision Mar 8, 1990
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
46
Review Days
85

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Basic Information

Device Name
SPACELABS MODEL 90480 EEG MODULE
K Number
K896942
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Spacelabs, Inc.
Date Received
December 13, 1989
Decision Date
March 8, 1990
Product Code
GWQ
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
GWQ Full-Montage Standard Electroencephalograph

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Other Clearances by Spacelabs, Inc.

K Number Device Name
K954962 SPACELABS MEDICAL MULTIGAS ANALYZER
K951605 SPACELABS MEDICAL CASEMASTER INFORMATION MANAGEMENT SYSTEM
K950779 HEART RATE VARIABILITY SOFTWARE OPTION
K941165 COMET CAPNOGRAPH MODULE
K923788 SPACE LABS MODEL 90560
K912742 ESOPHAGEAL STETHOSCOPE TEMPERATURE PROBE
K913038 SPACELAB MODEL 90845 PCMS MULTIDISCLOSURE STATION
K905065 DEFIBRILLATOR LEAD ADAPTER
K910029 PATIENT CARE MANAGEMENT SYSTEM MODIFICATION
K896903 FIRST MEDIC MODEL 510
Search all 46 clearances from Spacelabs, Inc. →