FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BEHIND-THE-EAR MODEL 115 V AGC O W

K Number: K822655 · Decision Sep 14, 1982
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
1366
Applicant Total
26
Review Days
12

Basic Information

Device Name
BEHIND-THE-EAR MODEL 115 V AGC O W
K Number
K822655
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
DANAVOX, INC.
Date Received
September 2, 1982
Decision Date
September 14, 1982
Product Code
ESD
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
ESD Hearing Aid, Air-Conduction, Prescription

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