Astroscan, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Astroscan, Ltd. makes
Astroscan, Ltd. manufactures the ASTROSCAN 2100 Microtiter Plate Reader, a device designed for optical density measurements in microplate formats, commonly used in laboratory settings for applications such as ELISA assays, cell viability testing, and biochemical research.
The ASTROSCAN 2100 Microtiter Plate Reader is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Astroscan 2100 Microtiter Plate Reader Ref K881458
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Astroscan, Ltd. have in the registry?
The registry currently lists 1 device for Astroscan, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Astroscan, Ltd.'s devices?
Among its 1 most recently registered device, Astroscan, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Astroscan, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Astroscan, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Astroscan, Ltd. in the registry?
The most recently registered devices listed for Astroscan, Ltd. include ASTROSCAN 2100 MICROTITER PLATE READER.