Gillco, Inc.
Country not established
- Devices
- 1
What Gillco, Inc. makes
Gillco, Inc. manufactures the ECA, a device designed for endoscopic procedures, including the removal or treatment of polyps or lesions within the gastrointestinal tract.
The company’s portfolio is regulated under FDA’s Class I device classification, with the ECA listed via the 510(k) pathway. Gillco, Inc. is based in the United States.
Catalogue
Eca Ref K811397
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gillco, Inc. have in the registry?
The registry currently lists 1 device for Gillco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gillco, Inc.'s devices?
Among its 1 most recently registered device, Gillco, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Gillco, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gillco, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gillco, Inc. in the registry?
The most recently registered devices listed for Gillco, Inc. include ECA.