Graseby Medical, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 5
What Graseby Medical, Ltd. makes
Graseby Medical, Ltd. manufactures infusion pumps, including the 3000, 3100, 3400, and 9000 series models. The company also produces the patient-controlled syringe pump type 3300.
These devices are classified as Class II medical products and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
3000 Infusion Pump Ref K912193
Regimes: 510(k) Registry: 510(k)3100 Infusion Pump Ref K912192
Regimes: 510(k) Registry: 510(k)3400 Infusion Pump Ref K931318
Regimes: 510(k) Registry: 510(k)9000 Infusion Pump Ref K944721
Regimes: 510(k) Registry: 510(k)Patient Controlled Syringe Pump Type 3300 Ref K915270
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Graseby Medical, Ltd. have in the registry?
The registry currently lists 5 devices for Graseby Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Graseby Medical, Ltd.'s devices?
Among its 5 most recently registered devices, Graseby Medical, Ltd. has devices listed in FDA 510(k) (5 devices).
What risk classes do Graseby Medical, Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Graseby Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Graseby Medical, Ltd. in the registry?
The most recently registered devices listed for Graseby Medical, Ltd. include 3000 INFUSION PUMP, 3100 INFUSION PUMP, 3400 INFUSION PUMP and 9000 INFUSION PUMP.