Precision Acoustics Ind., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precision Acoustics Ind., Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Precision Acoustics Ind., Inc. has 9 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 9 cleared submissions from 1993 to 1994. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Precision Acoustics Ind., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Precision Acoustics Ind., Inc.
9 devices
Cleared
Sep 23, 1994
INTERACOUSTICS HEARING AID ANALYZER MS 40
Ear, Nose, Throat
60d
Cleared
Sep 16, 1994
INTERACOUSTICS CLINICAL AUDIOMETER
Ear, Nose, Throat
149d
Cleared
Aug 24, 1994
INTERACOUSTICS CLINICAL IMPEDANCE AUDIOMETER AZ26
Ear, Nose, Throat
121d
Cleared
Aug 24, 1994
INTERACOUSTICS AUTOMATIC IMPEDANCE AUDIOMETER
Ear, Nose, Throat
121d
Cleared
Aug 24, 1994
INTERACOUSTICS COMPUTER AUDIOMETER BA 20
Ear, Nose, Throat
57d
Cleared
Aug 17, 1994
INTERACOUSTICS CLINICAL AUDIOMETER
Ear, Nose, Throat
50d
Cleared
Jun 20, 1994
INTERACOUSTICS DIAGNOSTIC AUDIOMETER
Ear, Nose, Throat
56d
Cleared
May 23, 1994
INTERACOUSTICS. HEARING AID ANALYZER
Ear, Nose, Throat
39d
Cleared
Jul 13, 1993
ACOUSTIC ANALYZER AA30
Ear, Nose, Throat
175d