Kareco Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Kareco Intl., Inc. makes
Kareco Intl., Inc. manufactures manual wheelchairs designed for patient mobility and support, as well as intravenous (I.V.) stands with double-hook attachments for securing medical supplies.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Kareco Int'l Wheelchair Ref K843688
Regimes: 510(k) Registry: 510(k)Kareco Int'l - Dougle-Hook I.V. Stand Ref K845031
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kareco Intl., Inc. have in the registry?
The registry currently lists 2 devices for Kareco Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kareco Intl., Inc.'s devices?
Among its 2 most recently registered devices, Kareco Intl., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Kareco Intl., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kareco Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kareco Intl., Inc. in the registry?
The most recently registered devices listed for Kareco Intl., Inc. include KARECO INT'L WHEELCHAIR and KARECO INT'L - DOUGLE-HOOK I.V. STAND.