Hc Electronics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hc Electronics - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Hc Electronics has 10 FDA 510(k) cleared ear, nose, throat devices. Based in Walker, US.
Historical record: 10 cleared submissions from 1977 to 1981.
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 - Hc Electronics
10 devices
Cleared
Mar 04, 1981
STEREO AUDITORY TRAINER (MODEL PM228)
Ear, Nose, Throat
57d
Cleared
Jan 14, 1981
POST-AURICULAR HEARING AID (#PE830)
Ear, Nose, Throat
8d
Cleared
Feb 26, 1980
PHONIC EAR, MODEL 841L
Ear, Nose, Throat
11d
Cleared
Dec 15, 1978
HEARING AID, POST-AURICULAR
Ear, Nose, Throat
8d
Cleared
Jun 22, 1978
PHONIC EAR
Ear, Nose, Throat
14d
Cleared
Mar 21, 1978
PHONIC EAR
Ear, Nose, Throat
15d
Cleared
Jan 11, 1978
PHONIC MIRROR HANDIVOCIE MODEL 110
Gastroenterology & Urology
19d
Cleared
Jan 11, 1978
PHONIC MIRROR HANDIVOICE MODEL 120
Gastroenterology & Urology
19d
Cleared
Jul 29, 1977
POST-AURICULAR HEARING AID HC 880
Ear, Nose, Throat
7d
Cleared
Jul 29, 1977
GROUP AUDITORY TRAINER HC 431R
Ear, Nose, Throat
7d