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

MONTGOMERY NERVE STIMULATOR

K Number: K880720 · Decision May 20, 1988
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
94
Applicant Total
33
Review Days
87

Basic Information

Device Name
MONTGOMERY NERVE STIMULATOR
K Number
K880720
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1820
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
BOSTON MEDICAL PRODUCTS, INC.
Date Received
February 23, 1988
Decision Date
May 20, 1988
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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