Amcor Electronics, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Amcor Electronics, Ltd. makes
Amcor Electronics, Ltd. manufactures the KARYOTEC 100, a device designed for chromosomal analysis and karyotyping in clinical or research settings.
The KARYOTEC 100 is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Karyotec 100 Ref K872755
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Amcor Electronics, Ltd. have in the registry?
The registry currently lists 1 device for Amcor Electronics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amcor Electronics, Ltd.'s devices?
Among its 1 most recently registered device, Amcor Electronics, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Amcor Electronics, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Amcor Electronics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amcor Electronics, Ltd. in the registry?
The most recently registered devices listed for Amcor Electronics, Ltd. include KARYOTEC 100.