Marcon Hearing Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Marcon Hearing Instruments, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Marcon Hearing Instruments, Inc. has 10 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1979 to 1982.
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 - Marcon Hearing Instruments, Inc.
10 devices
Cleared
Dec 03, 1982
MODEL H 37E
Ear, Nose, Throat
11d
Cleared
May 05, 1982
MODEL IM9
Ear, Nose, Throat
21d
Cleared
Oct 30, 1979
MODEL H44-80 BEHIND THE EAR HEARING
Ear, Nose, Throat
50d
Cleared
Jul 17, 1979
MODEL CE-DM-II HEARING INSTRUMENT
Ear, Nose, Throat
29d
Cleared
Jul 05, 1979
MODEL H63, BEHIND-THE-EAR
Ear, Nose, Throat
59d
Cleared
May 16, 1979
MODEL H39C-BEHING-THE-EAR HEARING INSTRU
Gastroenterology & Urology
23d
Cleared
May 01, 1979
MODEL H58-BEHIND-THE-EAR HEARING INSTR.
Ear, Nose, Throat
21d
Cleared
May 01, 1979
BEHIND-THE-EAR HEARING INSTRUMENT, H56
Ear, Nose, Throat
19d
Cleared
May 01, 1979
BEHIND-THE-EAR HEARING INSTRUMENT, H54
Ear, Nose, Throat
18d
Cleared
May 01, 1979
BEHIND-THE-EAR, MODEL H37D
Ear, Nose, Throat
18d