Hearing Tech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hearing Tech, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Hearing Tech, Inc. has 11 FDA 510(k) cleared ear, nose, throat devices. Based in Minnetonka, US.
Historical record: 11 cleared submissions from 1985 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 - Hearing Tech, Inc.
11 devices
Cleared
Jun 24, 1994
HEARING TECH
Ear, Nose, Throat
85d
Cleared
Dec 08, 1992
ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM
Cardiovascular
81d
Cleared
Mar 08, 1991
543 SERIES BTE
Ear, Nose, Throat
79d
Cleared
Sep 05, 1990
ESCORT ITC
Ear, Nose, Throat
42d
Cleared
Jul 27, 1990
HERITAGE III (HTC) ITC TYPE HEARING AID
Ear, Nose, Throat
17d
Cleared
Mar 20, 1987
HEARTECH HFX, HEARING AID
Ear, Nose, Throat
24d
Cleared
Mar 11, 1987
ESCORT EC CUSTOM IN-THE-EAR HEARING AID
Ear, Nose, Throat
41d
Cleared
Jan 21, 1986
HEARTECH MODEL IN TECH
Ear, Nose, Throat
85d
Cleared
Sep 23, 1985
HEARTECH MODEL(HTC) (HERITAGE)
Ear, Nose, Throat
53d
Cleared
Sep 23, 1985
HEARTECH MODEL CH
Ear, Nose, Throat
53d
Cleared
Sep 23, 1985
HEARTECH MODEL ILLUSION
Ear, Nose, Throat
53d