Fluoro-Mold Co.
Country not established
- Devices
- 1
What Fluoro-Mold Co. makes
Fluoro-Mold Co. manufactures peritoneal dialysis catheters, which are implanted devices used for accessing the peritoneal cavity to facilitate fluid exchange during dialysis treatments.
The company’s products are regulated as Class II medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Peritoneal Dialysis Catheter Ref K771555
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fluoro-Mold Co. have in the registry?
The registry currently lists 1 device for Fluoro-Mold Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fluoro-Mold Co.'s devices?
Among its 1 most recently registered device, Fluoro-Mold Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Fluoro-Mold Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fluoro-Mold Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fluoro-Mold Co. in the registry?
The most recently registered devices listed for Fluoro-Mold Co. include PERITONEAL DIALYSIS CATHETER.