Labone, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Labone, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LABONE COCAINE METABOLITE MICRO-PLATE EIA, LABONE MICRO-PLATE COTININE EIA
2
Total
2
Cleared
0
Denied
Labone, Inc. has 2 FDA 510(k) cleared medical devices. Based in Lenexa, US.
Historical record: 2 cleared submissions from 2004 to 2004. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Labone, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Labone, Inc.
2 devices