B&K Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
B&K Medical - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
B&K Medical has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 4 cleared submissions from 1981 to 1996. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by B&K Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - B&K Medical
4 devices
Cleared
Feb 09, 1996
ULTRASOUND SCANNER 2002
Radiology
578d
Cleared
Jun 28, 1994
DIAGNOSTIC ULTRASOUND SYSTEM, TYPE 3535, MODIFIED
Radiology
589d
Cleared
Jun 24, 1994
DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535, MODIFIED
Radiology
372d
Cleared
Jan 02, 1981
K-KATH URETHRAL CATHETER INTRODUCER
Gastroenterology & Urology
46d