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

101M IN-THE-EAR

K Number: K823073 · Decision Jan 7, 1983
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
26
Review Days
80

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Basic Information

Device Name
101M IN-THE-EAR
K Number
K823073
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
October 19, 1982
Decision Date
January 7, 1983
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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Other Clearances by Danavox, Inc.

K Number Device Name
K940608 155 PP AGC-I
K851069 BODY TYPE HEARING AID 107S
K843791 BEHIND-THE-EAR 123 VTH
K833486 IN-THE-EAR HEARING AID MODEL
K832326 BEHIND-THE-EAR #123 AGCI
K832751 BEHIND-THE-EAR SERIES 125
K823531 BEHIND-THE-EAR HEARING AID #8003
K822619 BEHIND-THE-EAR MODEL 115PPPCW
K822655 BEHIND-THE-EAR MODEL 115 V AGC O W
K822387 BEHIND-THE-EAR MODEL SERIES 123
Search all 26 clearances from Danavox, Inc. →