Futumeds Sdn Bhd
MalaysiaFDA 510(k) applicant, unverified
- Devices
- 1
What Futumeds Sdn Bhd makes
Futumeds Sdn Bhd manufactures the Futumeds No Patient Contact Safety Lancet with PALS System, a sterile, single-use lancet designed for blood glucose monitoring without direct skin contact, reducing infection risks.
The device is classified as Class I under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Futumeds Sdn Bhd have in the registry?
The registry currently lists 1 device for Futumeds Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Futumeds Sdn Bhd's devices?
Among its 1 most recently registered device, Futumeds Sdn Bhd has devices listed in FDA 510(k) (1 device).
What risk classes do Futumeds Sdn Bhd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Futumeds Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Futumeds Sdn Bhd in the registry?
The most recently registered devices listed for Futumeds Sdn Bhd include FUTUMEDS NO PATIENT CONTACT SAFETY LANCET WITH PALS SYSTEM.