Hudson Kendale Assoc., Inc.
Country not established
- Devices
- 1
What Hudson Kendale Assoc., Inc. makes
Hudson Kendale Associates, Inc. manufactures a non-retention enema system designed for gastrointestinal procedures, including bowel preparation and irrigation.
The company’s product portfolio is regulated as Class II medical devices under FDA 510(k) clearance requirements and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Non-Retention Enema System Ref K781923
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hudson Kendale Assoc., Inc. have in the registry?
The registry currently lists 1 device for Hudson Kendale Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hudson Kendale Assoc., Inc.'s devices?
Among its 1 most recently registered device, Hudson Kendale Assoc., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hudson Kendale Assoc., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hudson Kendale Assoc., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hudson Kendale Assoc., Inc. in the registry?
The most recently registered devices listed for Hudson Kendale Assoc., Inc. include NON-RETENTION ENEMA SYSTEM.