Medi Point, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Medi Point, Inc. makes
Medi Point, Inc. manufactures the MEDIPOINT MULTI-SAMPLE BLOOD COLLECTING NEEDLE, a medical device used for collecting blood samples.
The device is classified as Class II and is listed in the FDA 510(k) registry. Medi Point, Inc. is based in the US.
Catalogue
Medipoint Ref K982961
Regimes: 510(k) Registry: 510(k)Medipoint Multi-Sample Blood Collecting Needle Ref K861560
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medi Point, Inc. have in the registry?
The registry currently lists 2 devices for Medi Point, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medi Point, Inc.'s devices?
Among its 2 most recently registered devices, Medi Point, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medi Point, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medi Point, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medi Point, Inc. in the registry?
The most recently registered devices listed for Medi Point, Inc. include MEDIPOINT and MEDIPOINT MULTI-SAMPLE BLOOD COLLECTING NEEDLE.