Whittaker Bioproducts, Inc.
United StatesFDA applicant, unverified
- Devices
- 30
What Whittaker Bioproducts, Inc. makes
Whittaker Bioproducts, Inc. manufactures diagnostic test kits and fluorescent monoclonal antibodies for detecting viral and bacterial infections, including adenovirus, herpes simplex virus (HSV), cytomegalovirus (CMV), Epstein-Barr virus (EBV), Lyme disease, mumps, respiratory syncytial virus (RSV), and *Helicobacter pylori*. Products include immunofluorescence assay (FIAX) test kits and fluorescently labeled immunoglobulin G (IgG) antibodies for laboratory use.
The company’s portfolio includes Class I and Class II in vitro diagnostic devices, authorised through FDA 510(k) clearances. Devices are listed in the FDA’s 510(k) database, and the company operates from the United States.
Catalogue
Search and filter all 30 devicesFrequently asked questions
How many devices does Whittaker Bioproducts, Inc. have in the registry?
The registry currently lists 30 devices for Whittaker Bioproducts, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Whittaker Bioproducts, Inc.'s devices?
Among its 30 most recently registered devices, Whittaker Bioproducts, Inc. has devices listed in FDA 510(k) (30 devices).
What risk classes do Whittaker Bioproducts, Inc.'s devices fall under?
Among its 30 most recently registered devices, the classes recorded for Whittaker Bioproducts, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Whittaker Bioproducts, Inc. in the registry?
The most recently registered devices listed for Whittaker Bioproducts, Inc. include MURINE MONOCLONAL ANTI-ADENOVIRUS IGG, EB VCA STAT M TEST KIT, FITC MURINE MONOCLONAL ANTI-HSV BIVALENT IGG and FIAX TEST KIT FOR LYME DISEASE ANTIBODIES.