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

INVOTEC LARYNGEAL ELECTRODE

K Number: K122040 · Decision Oct 31, 2013
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
96
Applicant Total
16
Review Days
476

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Basic Information

Device Name
INVOTEC LARYNGEAL ELECTRODE
K Number
K122040
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1820
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Invotec International, Inc.
Date Received
July 12, 2012
Decision Date
October 31, 2013
Product Code
ETN
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ETN Stimulator, Nerve

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K971000 EPISTAXIS NASAL PACK
K930114 TRACHEOSTOMY T-TUBE
K911041 INVOTEC X-RAY CASSETTE EQUIPMENT DRAPE
K911040 INVOTEC MICROSCOPE DRAPE
K911039 INVOTEC EAR DRAPE
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