Handylab, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Handylab, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HANDYLAB GBS ASSAY, HANDYLAB JAGUAR INSTRUMENT, HANDYLAB DNA EXTRACTION STRIP, HANDYLAB E3 EXTRACTION REAGENT, HANDYLAB
1
Total
1
Cleared
0
Denied
Handylab, Inc. has 1 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Handylab, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Handylab, Inc.
1 devices