Algotec Systems, Ltd.
IsraelFDA applicant, unverified
- Devices
- 5
What Algotec Systems, Ltd. makes
Algotec Systems, Ltd. manufactures Mediprime and Pro Vision devices, including modifications to Mediprime.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Mdification To Mediprime Ref K033013
Regimes: 510(k) Registry: 510(k)Pro Vision Ref K980648
Regimes: 510(k) Registry: 510(k)Mediprime Ref K002894
Regimes: 510(k) Registry: 510(k)Modification To Mediprime Ref K023936
Regimes: 510(k) Registry: 510(k)Pro Vision Ref K954678
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Algotec Systems, Ltd. have in the registry?
The registry currently lists 5 devices for Algotec Systems, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Algotec Systems, Ltd.'s devices?
Among its 5 most recently registered devices, Algotec Systems, Ltd. has devices listed in FDA 510(k) (5 devices).
What risk classes do Algotec Systems, Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Algotec Systems, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Algotec Systems, Ltd. in the registry?
The most recently registered devices listed for Algotec Systems, Ltd. include MDIFICATION TO MEDIPRIME, PRO VISION, MEDIPRIME and MODIFICATION TO MEDIPRIME.