Preserve
Country not established
- Devices
- 1
What Preserve makes
Preserve manufactures the SECUTAINER, a device designed for the secure containment and transport of biological specimens, ensuring sample integrity and compliance with handling protocols.
The SECUTAINER is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance pathway. The company is based in the United States.
Catalogue
Secutainer Ref K902709
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Preserve have in the registry?
The registry currently lists 1 device for Preserve. Devices recorded under merged duplicate company entries are counted once.
Which registries list Preserve's devices?
Among its 1 most recently registered device, Preserve has devices listed in FDA 510(k) (1 device).
What risk classes do Preserve's devices fall under?
Among its 1 most recently registered device, the classes recorded for Preserve's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Preserve in the registry?
The most recently registered devices listed for Preserve include SECUTAINER.