Eischoco, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Eischoco, Inc. makes
Eischoco, Inc. manufactures intermittent compression boots designed for over-the-counter use and intermittent compression systems for venous circulation support.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Intermittent Compression Boot For Otc Ref K991921
Regimes: 510(k) Registry: 510(k)Intermittent Compressor System Ref K964957
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eischoco, Inc. have in the registry?
The registry currently lists 2 devices for Eischoco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eischoco, Inc.'s devices?
Among its 2 most recently registered devices, Eischoco, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Eischoco, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Eischoco, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eischoco, Inc. in the registry?
The most recently registered devices listed for Eischoco, Inc. include INTERMITTENT COMPRESSION BOOT FOR OTC and INTERMITTENT COMPRESSOR SYSTEM.