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

DEEG-LITE

K Number: K972202 · Decision Jul 23, 1997
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
12
Review Days
42

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Basic Information

Device Name
DEEG-LITE
K Number
K972202
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Grass-Telefactor Product Group
Date Received
June 11, 1997
Decision Date
July 23, 1997
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

Similar 510(k) Clearances

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

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Other Clearances by Grass-Telefactor Product Group

K Number Device Name
K992291 H20- TETHERED OPTION
K974583 DEEGLITE
K974587 H2O
K925838 TELEFACTOR D/EEG-32
K884937 BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDING
K870432 A1-A2 AMBULATORY EEG CASSETTE RECORDER
K871480 STD-228 SPECTRAL TREND DISPLAY
K870450 SZAC-16 SEIZURE ANALYSIS COMPUTER
K870381 DD-VCR-64
K860219 SASSSY SEMI AUTOMATIC SLEEP SCORING SYSTEM
Search all 12 clearances from Grass-Telefactor Product Group →