Pharmetrix, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Pharmetrix, Inc. makes
Pharmetrix, Inc. manufactures infusion pumps, including the Pharmetrix MiniPump Model 5120 and Pharmetrix MediPump Model 524, designed for controlled delivery of fluids in clinical settings.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Pharmetrix Minipump Model 5120 Ref K924603
Regimes: 510(k) Registry: 510(k)Pharmetrix Medipump Model 524 Ref K915407
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pharmetrix, Inc. have in the registry?
The registry currently lists 2 devices for Pharmetrix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pharmetrix, Inc.'s devices?
Among its 2 most recently registered devices, Pharmetrix, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pharmetrix, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pharmetrix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pharmetrix, Inc. in the registry?
The most recently registered devices listed for Pharmetrix, Inc. include PHARMETRIX MINIPUMP MODEL 5120 and PHARMETRIX MEDIPUMP MODEL 524.