Kendro Laboratory Products, L.P. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kendro Laboratory Products, L.P. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Kendro Laboratory Products, L.P. has 2 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 2 cleared submissions from 2000 to 2003. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Kendro Laboratory Products, L.P. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kendro Laboratory Products, L.P.
2 devices