Casco-Nerl Diagnostics Corporation (Maine)
United StatesFDA applicant, unverified
- Devices
- 3
What Casco-Nerl Diagnostics Corporation (Maine) makes
Casco-Nerl Diagnostics Corporation produces laboratory controls and calibration verification devices for thyroid assays, including chemistry controls at multiple levels and calibration verification tools for thyroid hormone measurements.
These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Modification To Document Thyroid Cal.ver Ref K993014
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Document Thyroid Cal*ver Ref K992034
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Casco-Nerl Diagnostics Corporation (Maine) have in the registry?
The registry currently lists 3 devices for Casco-Nerl Diagnostics Corporation (Maine). Devices recorded under merged duplicate company entries are counted once.
Which registries list Casco-Nerl Diagnostics Corporation (Maine)'s devices?
Among its 3 most recently registered devices, Casco-Nerl Diagnostics Corporation (Maine) has devices listed in FDA 510(k) (3 devices).
What risk classes do Casco-Nerl Diagnostics Corporation (Maine)'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Casco-Nerl Diagnostics Corporation (Maine)'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Casco-Nerl Diagnostics Corporation (Maine) in the registry?
The most recently registered devices listed for Casco-Nerl Diagnostics Corporation (Maine) include MODIFICATION TO DOCUMENT THYROID CAL.VER, DOCUMENT ASSAYED CHEMISTRY CONTROL, LEVELS 1, 2 AND3 and DOCUMENT THYROID CAL*VER.