Active Electronics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Active Electronics, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Active Electronics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Blaine, US.
Historical record: 7 cleared submissions from 1991 to 1994. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Active Electronics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Active Electronics, Inc.
7 devices
Cleared
Dec 21, 1994
ACTIVE MODEL CIC
Ear, Nose, Throat
56d
Cleared
Feb 28, 1991
ACTIVE MODEL AST CUSTOM ITE HEARING AID
Ear, Nose, Throat
8d
Cleared
Feb 28, 1991
ACTIVE MODEL ALP LOW PROFILE ITE HEARING AID
Ear, Nose, Throat
8d
Cleared
Feb 28, 1991
ACTIVE MODEL AHS HALF SHELL ITE HEARING AID
Ear, Nose, Throat
8d
Cleared
Feb 28, 1991
ACTIVE MODEL ACA CUSTOM CANAL ITE HEARING AID
Ear, Nose, Throat
8d
Cleared
Feb 28, 1991
ACTIVE MODEL AMC MINI CANAL ITE HEARING AID
Ear, Nose, Throat
8d
Cleared
Feb 28, 1991
ACTIVE MODEL AHX HELIX ITE HEARING AID
Ear, Nose, Throat
8d