Mimosa Acoustics, Inc. is one of 5240 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mimosa Acoustics, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Mimosa Acoustics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Champaign, US.
Historical record: 4 cleared submissions from 1998 to 2013. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Mimosa Acoustics, Inc. Filter by specialty or product code using the sidebar.
Mimosa Acoustics, Inc. — FDA 510(k) Products and Clearance History
4 devices
Cleared
Mar 28, 2013
OTOSTAT DPOAE + MEPA MEASUREMENT SYSTEM
Ear, Nose, Throat
125d
Cleared
Jan 04, 2007
HEARID+TE TRANSIENT-EVOKED OTOACOUSTIC EMISSIONS ANALYZER
Ear, Nose, Throat
59d
Cleared
Feb 10, 2006
HEARID WIDEBAND MIDDLE EAR POWER ANALYZER
Ear, Nose, Throat
85d
Cleared
May 20, 1998
CUB DIS II DPOAE MEASUREMENT SYSTEM
Ear, Nose, Throat
27d