S.P.O. Medical Equipment, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What S.P.O. Medical Equipment, Ltd. makes
S.P.O. Medical Equipment, Ltd. manufactures pulse oximetry devices, including finger-based and wristwatch-style models designed for monitoring oxygen saturation and pulse rate in clinical and patient-monitoring settings.
The company’s portfolio is regulated under FDA’s Class II device classification, with products listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does S.P.O. Medical Equipment, Ltd. have in the registry?
The registry currently lists 1 device for S.P.O. Medical Equipment, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list S.P.O. Medical Equipment, Ltd.'s devices?
Among its 1 most recently registered device, S.P.O. Medical Equipment, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do S.P.O. Medical Equipment, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for S.P.O. Medical Equipment, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from S.P.O. Medical Equipment, Ltd. in the registry?
The most recently registered devices listed for S.P.O. Medical Equipment, Ltd. include PULSEOX 5500 FINGER DEVICE, PULSEOX 7500 WRISTWATCH DEVICE.