Danavox, Inc. - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
FDA 510(k) Regulatory Record - Danavox, Inc. Ear, Nose, Throat ✕
26 devices
Cleared
May 04, 1994
155 PP AGC-I
Ear, Nose, Throat
79d
Cleared
Jun 05, 1985
BODY TYPE HEARING AID 107S
Ear, Nose, Throat
79d
Cleared
Nov 09, 1984
BEHIND-THE-EAR 123 VTH
Ear, Nose, Throat
43d
Cleared
Jun 22, 1984
IN-THE-EAR HEARING AID MODEL
Ear, Nose, Throat
259d
Cleared
Sep 29, 1983
BEHIND-THE-EAR #123 AGCI
Ear, Nose, Throat
76d
Cleared
Sep 29, 1983
BEHIND-THE-EAR SERIES 125
Ear, Nose, Throat
45d
Cleared
Jan 07, 1983
101M IN-THE-EAR
Ear, Nose, Throat
80d
Cleared
Dec 15, 1982
BEHIND-THE-EAR HEARING AID #8003
Ear, Nose, Throat
16d
Cleared
Sep 14, 1982
BEHIND-THE-EAR MODEL 115PPPCW
Ear, Nose, Throat
12d
Cleared
Sep 14, 1982
BEHIND-THE-EAR MODEL 115 V AGC O W
Ear, Nose, Throat
12d
Cleared
Aug 19, 1982
BEHIND-THE-EAR MODEL SERIES 123
Ear, Nose, Throat
10d
Cleared
Nov 06, 1981
BEHIND-THE-EAR MODEL 115
Ear, Nose, Throat
17d