Siemens Heatlhcare Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
- Regimes: 510(k) Registry: 510(k)
Dimension Visa HBA1C, Model K3105A Ref K102045
Regimes: 510(k) Registry: 510(k)Dimension Mycophenolic Acid (Mpat) Flex Reagent Cartridge, Dimension Mycophenolic Acid Calibrator (Mpat Cal) Ref K102772
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Siemens Heatlhcare Diagnostics, Inc. have in the registry?
The registry currently lists 3 devices for Siemens Heatlhcare Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Siemens Heatlhcare Diagnostics, Inc.'s devices?
Among its 3 most recently registered devices, Siemens Heatlhcare Diagnostics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Siemens Heatlhcare Diagnostics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Siemens Heatlhcare Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Siemens Heatlhcare Diagnostics, Inc. in the registry?
The most recently registered devices listed for Siemens Heatlhcare Diagnostics, Inc. include ADVIA CENTAUR CALIBRATOR 30, MODELS 10379811/10379810, DIMENSION VISA HBA1C, MODEL K3105A and DIMENSION MYCOPHENOLIC ACID (MPAT) FLEX REAGENT CARTRIDGE, DIMENSION MYCOPHENOLIC ACID CALIBRATOR (MPAT CAL).