Danavox, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Danavox, Inc. - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
Danavox, Inc. has 26 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.
Historical record: 26 cleared submissions from 1977 to 1994.
Browse the complete list of FDA 510(k) cleared ear, nose, throat devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Danavox, Inc.
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