Flint Laboratories Div. Travenol
Country not established
- Devices
- 1
What Flint Laboratories Div. Travenol makes
Flint Laboratories (Travenol Division) manufactures the FNA Thyroid Biopsy Kit, a sterile, single-use device designed for fine-needle aspiration procedures of thyroid nodules to aid in cytological diagnosis.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance for market authorisation. The products are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Fna Thyroid Biopsy Kit Ref K870863
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Flint Laboratories Div. Travenol have in the registry?
The registry currently lists 1 device for Flint Laboratories Div. Travenol. Devices recorded under merged duplicate company entries are counted once.
Which registries list Flint Laboratories Div. Travenol's devices?
Among its 1 most recently registered device, Flint Laboratories Div. Travenol has devices listed in FDA 510(k) (1 device).
What risk classes do Flint Laboratories Div. Travenol's devices fall under?
Among its 1 most recently registered device, the classes recorded for Flint Laboratories Div. Travenol's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Flint Laboratories Div. Travenol in the registry?
The most recently registered devices listed for Flint Laboratories Div. Travenol include FNA THYROID BIOPSY KIT.