Cbc Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cbc Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Cbc Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1983 to 1983. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Cbc Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cbc Corp.
5 devices
Cleared
Aug 31, 1983
AUTO-TENS MODEL V
Neurology
44d
Cleared
Mar 07, 1983
AUTO-TENS MODEL III DUAL CHANNEL REPLACE
Neurology
108d
Cleared
Feb 07, 1983
AUTO-TENS MODEL I DISPOS. SINGLE CHAN
Neurology
80d
Cleared
Feb 02, 1983
AUTO-TENS MODEL IV -DUAL CHANNEL FULL
Neurology
75d
Cleared
Feb 02, 1983
AUTO-TENS MODEL II SINGLE CHANNEL
Neurology
75d