IBM Israel, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What IBM Israel, Ltd. makes
Ibm Israel, Ltd. develops an integrated digital medical record system designed to streamline patient data management and improve clinical workflow efficiency.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Integrated Digital Medical Record (Idmr) Ref K993338
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ibm Israel, Ltd. have in the registry?
The registry currently lists 1 device for Ibm Israel, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ibm Israel, Ltd.'s devices?
Among its 1 most recently registered device, Ibm Israel, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ibm Israel, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ibm Israel, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ibm Israel, Ltd. in the registry?
The most recently registered devices listed for Ibm Israel, Ltd. include INTEGRATED DIGITAL MEDICAL RECORD (IDMR).