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

CADWELL LIMB MOVEMENT MODULE

K Number: K040986 · Decision Jul 1, 2004
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
16
Applicant Total
46
Review Days
77

Basic Information

Device Name
CADWELL LIMB MOVEMENT MODULE
K Number
K040986
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 15, 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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