C B Bard, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
C B Bard, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Pristine Long-Term Hemodialysis Catheter
1
Total
0
Cleared
0
Denied
C B Bard, Inc. has 0 FDA 510(k) cleared medical devices. Based in Tempe, US.
Last cleared in 2021. Active since 2021. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by C B Bard, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - C B Bard, Inc.
1 devices