Eagle Endoscopic, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Eagle Endoscopic, Inc. makes
Eagle Endoscopic, Inc. manufactures endoscopic specimen retrieval bags and slush pan drapes, designed for use in minimally invasive surgical procedures to safely contain and transport tissue samples and maintain sterile field conditions during cryotherapy applications.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Eagle Endo Specimen Retrieval Bag Ref K001264
Regimes: 510(k) Registry: 510(k)Eei Slush Pan Drape Ref K001994
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eagle Endoscopic, Inc. have in the registry?
The registry currently lists 2 devices for Eagle Endoscopic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eagle Endoscopic, Inc.'s devices?
Among its 2 most recently registered devices, Eagle Endoscopic, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Eagle Endoscopic, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Eagle Endoscopic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eagle Endoscopic, Inc. in the registry?
The most recently registered devices listed for Eagle Endoscopic, Inc. include EAGLE ENDO SPECIMEN RETRIEVAL BAG and EEI SLUSH PAN DRAPE.