Siemens Helathcare Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
Microscan Dried Gram-Postive Mic/Combo Panels Ref K131275
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Siemens Helathcare Diagnostics, Inc. have in the registry?
The registry currently lists 2 devices for Siemens Helathcare Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Siemens Helathcare Diagnostics, Inc.'s devices?
Among its 2 most recently registered devices, Siemens Helathcare Diagnostics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Siemens Helathcare Diagnostics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Siemens Helathcare Diagnostics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Siemens Helathcare Diagnostics, Inc. in the registry?
The most recently registered devices listed for Siemens Helathcare Diagnostics, Inc. include MICROSCAN DRIED GRAM-POSTIVE MIC/COMBO PANELS and IMMULITE 2000 ANTI-TG AB CALIBRATION VERIFICATION MATERIAL, IMMULITE 2000 ANTI-TPO AB CALIBRATION VERIFICATIN MATERIAL.