Webster Enterprises, Inc.
Country not established
- Devices
- 1
What Webster Enterprises, Inc. makes
Webster Enterprises, Inc. manufactures sterile surgical drape packs designed for use in surgical procedures to maintain a clean field and reduce contamination risk.
The company’s products are regulated as Class II 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
Surgical Drape Pack Ref K864899
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Webster Enterprises, Inc. have in the registry?
The registry currently lists 1 device for Webster Enterprises, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Webster Enterprises, Inc.'s devices?
Among its 1 most recently registered device, Webster Enterprises, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Webster Enterprises, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Webster Enterprises, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Webster Enterprises, Inc. in the registry?
The most recently registered devices listed for Webster Enterprises, Inc. include SURGICAL DRAPE PACK.