Kronus Market Development Associates, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 11
What Kronus Market Development Associates, Inc. makes
The company manufactures diagnostic assay kits for detecting specific autoantibodies and antibodies, including insulin autoantibody (IAA), voltage-gated calcium channel (VGCC), zinc transporter 8 (ZNT8), steroid 21-hydroxylase, glutamic acid decarboxylase, acetylcholine receptor (AChR), and thyroid-stimulating hormone receptor (TSH) antibodies. These kits use radioimmunoassay (RIA) or enzyme-linked immunosorbent assay (ELISA) methods for clinical testing.
All listed products fall under FDA Class II devices and are authorised via the 510(k) pathway. The company’s assays are registered with the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Kronus Market Development Associates, Inc. have in the registry?
The registry currently lists 11 devices for Kronus Market Development Associates, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kronus Market Development Associates, Inc.'s devices?
Among its 11 most recently registered devices, Kronus Market Development Associates, Inc. has devices listed in FDA 510(k) (11 devices).
What risk classes do Kronus Market Development Associates, Inc.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Kronus Market Development Associates, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kronus Market Development Associates, Inc. in the registry?
The most recently registered devices listed for Kronus Market Development Associates, Inc. include KRONUS IA-2 AUTOANTIBODY RIA ASSAY KIT, KRONUS INSULIN AUTOANTIBODY (IAA) ASSAY KIT, KRONUS GAD AUTOANTIBODY ELISA ASSAY KIT and TSH RECEPTOR ANTIBODY (TRAB) COATED TUBE (CT) ASSAY KIT.