Med-Conduit, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Med-Conduit, Inc. makes
Med-Conduit, Inc. manufactures hemodialysis catheters, including the HEMOCATH and HEMOCATH II for vascular access, as well as peritoneal dialysis catheters (PD CATH) designed for fluid exchange in peritoneal dialysis procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Hemocath Ref K043292
Regimes: 510(k) Registry: 510(k)Hemocath Ii Ref K062901
Regimes: 510(k) Registry: 510(k)Pd Cath Ref K053123
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Med-Conduit, Inc. have in the registry?
The registry currently lists 3 devices for Med-Conduit, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med-Conduit, Inc.'s devices?
Among its 3 most recently registered devices, Med-Conduit, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Med-Conduit, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Med-Conduit, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Med-Conduit, Inc. in the registry?
The most recently registered devices listed for Med-Conduit, Inc. include HEMOCATH, HEMOCATH II and PD CATH.