Pro. Duct Health, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Pro. Duct Health, Inc. makes
Pro. Duct Health, Inc. manufactures the PRO.DUCT HEALTH MICRO-STYLET (STY01), a precision guidewire for endoscopic procedures, and the PRO.DUCT CATHETER (CTH03), designed for ductal access and drainage in biliary or pancreatic applications.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company operates within the United States.
Catalogue
Pro.duct Health Micro-Stylet, Model STY01 Ref K001098
Regimes: 510(k) Registry: 510(k)Pro.duct Catheter, Model CTH03 Ref K000135
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pro. Duct Health, Inc. have in the registry?
The registry currently lists 2 devices for Pro. Duct Health, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pro. Duct Health, Inc.'s devices?
Among its 2 most recently registered devices, Pro. Duct Health, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pro. Duct Health, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pro. Duct Health, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pro. Duct Health, Inc. in the registry?
The most recently registered devices listed for Pro. Duct Health, Inc. include PRO.DUCT HEALTH MICRO-STYLET, MODEL STY01 and PRO.DUCT CATHETER, MODEL CTH03.