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

EASYNET BODY POSITION MODULE

K Number: K040932 · Decision Jul 1, 2004
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
18
Applicant Total
46
Review Days
83

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Basic Information

Device Name
EASYNET BODY POSITION MODULE
K Number
K040932
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5050
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cadwell Laboratories, Inc.
Date Received
April 9, 2004
Decision Date
July 1, 2004
Product Code
LEL
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
LEL Device, Sleep Assessment

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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
K971214 KILOWIN
K962455 FOUR-CHANNEL PREAMPLIFIER
K962457 TWO-CHANNEL PREAMPLIFIER
K962458 CADWELL FOUR-/EIGHT-CHANNEL PREAMPLIFIER
K946094 CADWELL EASY AMBULATORY EEG
K933808 EEG CUP ELECTRODE
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