Theodore Barash is one of 25625 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Theodore Barash - FDA 510(k) Cleared Devices
Recent clearances: BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE
1
Total
1
Cleared
0
Denied
Theodore Barash has 1 FDA 510(k) cleared medical devices. Based in Delray Beach, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Theodore Barash Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Theodore Barash
1 devices