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

CADWELL EASY AMBULATORY EEG

K Number: K946094 · Decision Sep 12, 1995
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
46
Review Days
272

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CADWELL EASY AMBULATORY EEG
K Number
K946094
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cadwell Laboratories, Inc.
Date Received
December 14, 1994
Decision Date
September 12, 1995
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.

View all

Other Clearances by Cadwell Laboratories, Inc.

K Number Device Name
K061706 CADWELL EASYNET OXIMETER MODULE
K061705 CADWELL EASYNET NASAL PRESSURE MODULE
K042350 TES-1 CONSTANT VOLTAGE ELECTRICAL STIMULATOR
K040986 CADWELL LIMB MOVEMENT MODULE
K040932 EASYNET BODY POSITION MODULE
K971214 KILOWIN
K962455 FOUR-CHANNEL PREAMPLIFIER
K962457 TWO-CHANNEL PREAMPLIFIER
K962458 CADWELL FOUR-/EIGHT-CHANNEL PREAMPLIFIER
K933808 EEG CUP ELECTRODE
Search all 46 clearances from Cadwell Laboratories, Inc. →