Medfusion, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Medfusion, Inc. makes
Medfusion, Inc. manufactures ambulatory infusion pumps, including syringe infusion pumps and modified versions like the WalkMed 400 and Model 3001. Their portfolio also includes the Model 2001 with modifications, designed for continuous or intermittent drug delivery in outpatient settings.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
Ambulatory Infusion Pump Ref K890862
Regimes: 510(k) Registry: 510(k)Modified Walkmed 400 Ref K905783
Regimes: 510(k) Registry: 510(k)Model 3001 Syringe Infusion Pump Ref K901755
Regimes: 510(k) Registry: 510(k)Syringe Infusion Pump Ref K890120
Regimes: 510(k) Registry: 510(k)Model 2001, Modification Ref K905029
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medfusion, Inc. have in the registry?
The registry currently lists 5 devices for Medfusion, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medfusion, Inc.'s devices?
Among its 5 most recently registered devices, Medfusion, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Medfusion, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Medfusion, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medfusion, Inc. in the registry?
The most recently registered devices listed for Medfusion, Inc. include AMBULATORY INFUSION PUMP, MODIFIED WALKMED 400, MODEL 3001 SYRINGE INFUSION PUMP and SYRINGE INFUSION PUMP.