Vanguard Diagnostic Systems
Country not established
- Devices
- 2
What Vanguard Diagnostic Systems makes
Vanguard Diagnostic Systems manufactures unassayed control sera for laboratory use, including bovine normal and abnormal reference standards. These products are designed to support quality assurance in diagnostic testing environments by providing consistent, pre-characterized samples for calibration and validation purposes.
The company’s portfolio is classified under Class I medical devices and is listed in the FDA’s 510(k) registry. The products are intended for use in the United States, where regulatory compliance aligns with FDA requirements for laboratory reagents.
Catalogue
Unassayed Control Serum, Abnormal (Bovine) Ref K872303
Regimes: 510(k) Registry: 510(k)Unassayed Control Serum, Normal (Bovine) Ref K872304
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vanguard Diagnostic Systems have in the registry?
The registry currently lists 2 devices for Vanguard Diagnostic Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vanguard Diagnostic Systems's devices?
Among its 2 most recently registered devices, Vanguard Diagnostic Systems has devices listed in FDA 510(k) (2 devices).
What risk classes do Vanguard Diagnostic Systems's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vanguard Diagnostic Systems's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Vanguard Diagnostic Systems in the registry?
The most recently registered devices listed for Vanguard Diagnostic Systems include UNASSAYED CONTROL SERUM, ABNORMAL (BOVINE) and UNASSAYED CONTROL SERUM, NORMAL (BOVINE).