Ercons, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 6
Catalogue
Erco-Ribbon Ref K981343
510(k) 510(k)Erco-Vac Ref K972537
510(k) 510(k)Erco-Ribbon Ref K972353
510(k) 510(k)Erco-Vac Ref K981357
510(k) 510(k)Erco-Ribbon -C Ref K990008
510(k) 510(k)Erco-Vac -C Ref K990006
510(k) 510(k)
Frequently asked questions
How many devices does Ercons, Inc. have in the registry?
The registry currently lists 6 devices for Ercons, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ercons, Inc.'s devices?
Among its 6 most recently registered devices, Ercons, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Ercons, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Ercons, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ercons, Inc. in the registry?
The most recently registered devices listed for Ercons, Inc. include ERCO-RIBBON, ERCO-VAC, ERCO-RIBBON -C and ERCO-VAC -C.