FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

TD50 ELECTROMYOGRAPH

K Number: K935017 · Decision Jul 28, 1994
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
26
Applicant Total
15
Review Days
282

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Basic Information

Device Name
TD50 ELECTROMYOGRAPH
K Number
K935017
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1550
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medelec Intl. Corp.
Date Received
October 19, 1993
Decision Date
July 28, 1994
Product Code
JXE
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
JXE Device, Nerve Conduction Velocity Measurement

Similar 510(k) Clearances

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Other Clearances by Medelec Intl. Corp.

K Number Device Name
K961013 DISPOSABLE NEEDLE ELECTRODE
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K920127 ELECTROENCEPHALOGRAPH RECORDING SYSTEM
K912775 SAPPHIRE 4ME EMG/EP SYSTEM
K865106 PROPHYLACTIC (CONDOM) MR. JOHNNY
K863491 BLOOD SPECIMEN COLLECTION DEVICES
K854622 PROPHYLACTIC (CONDOM)
K854562 CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I
K854860 BLADES, SCALPEL CARBON STEET
K854858 SCALPEL HANDLE
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