Mcpherson Enterprises, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Mcpherson Enterprises, Inc. makes
McPherson Enterprises, Inc. manufactures modifications to the Smithwick Carotid Shunt, a vascular device used in carotid artery procedures, and produces multi-lumen intravenous catheters for fluid administration and monitoring.
The company’s portfolio consists of Class II medical devices, all of which are authorised via the FDA’s 510(k) pathway. These devices are listed under the US regulatory framework and are based in the United States.
Catalogue
Modification To: Smithwick Carotid Shunt Ref K061484
Regimes: 510(k) Registry: 510(k)Multi-Lumen Intravenous Catheter Ref K823565
Regimes: 510(k) Registry: 510(k)Smithwick Carotid Shunt Ref K062474
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mcpherson Enterprises, Inc. have in the registry?
The registry currently lists 3 devices for Mcpherson Enterprises, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mcpherson Enterprises, Inc.'s devices?
Among its 3 most recently registered devices, Mcpherson Enterprises, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Mcpherson Enterprises, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mcpherson Enterprises, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mcpherson Enterprises, Inc. in the registry?
The most recently registered devices listed for Mcpherson Enterprises, Inc. include MODIFICATION TO: SMITHWICK CAROTID SHUNT, MULTI-LUMEN INTRAVENOUS CATHETER and SMITHWICK CAROTID SHUNT.