Amdl, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Amdl, Inc. makes
Amdl, Inc. makes the PyloriProbe and the AMDL-ELISA DR-70 (FDP) immunoassay, model DR2101.
These devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Pyloriprobe Ref K981396
Regimes: 510(k) Registry: 510(k)Amdl-Elisa Dr-70 (Fdp) Immunoassay, Model DR2101 Ref K072901
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Amdl, Inc. have in the registry?
The registry currently lists 2 devices for Amdl, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amdl, Inc.'s devices?
Among its 2 most recently registered devices, Amdl, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Amdl, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Amdl, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amdl, Inc. in the registry?
The most recently registered devices listed for Amdl, Inc. include PYLORIPROBE and AMDL-ELISA DR-70 (FDP) IMMUNOASSAY, MODEL DR2101.