Micro-Ear Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Micro-Ear Technology, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Micro-Ear Technology, Inc. has 5 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Historical record: 5 cleared submissions from 1993 to 2004. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Micro-Ear Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Micro-Ear Technology, Inc.
5 devices
Cleared
Jul 01, 2004
REFUGE SOUND GENERATOR
Ear, Nose, Throat
48d
Cleared
Jul 23, 1997
MERIDIAN DSP
Ear, Nose, Throat
29d
Cleared
Jun 06, 1997
POWER D, TRU 5, PERSONA, PERSONA CHOICE, MERIDIAN
Ear, Nose, Throat
88d
Cleared
Feb 11, 1997
SUPER K-AMP, EZ-COMPRESSION, TRIM-PRO, HF-PRO, ENVIRO-PRO, COMPRESSION-PRO,...
Ear, Nose, Throat
83d
Cleared
Dec 27, 1993
MICRO-TECH TRU CANAL
Ear, Nose, Throat
125d