B & L Ent. Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
B & L Ent. Co. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
B & L Ent. Co. has 2 FDA 510(k) cleared medical devices. Based in Campbell, US.
Historical record: 2 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by B & L Ent. Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - B & L Ent. Co.
2 devices