Bruker Medical Imaging, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 7
What Bruker Medical Imaging, Inc. makes
Bruker Medical Imaging, Inc. manufactures magnetic resonance imaging (MRI) systems, including whole-body scanners and angiography imaging accessories for head and chest applications. Their portfolio includes modified MRI systems like the BMT-1100 and R-28 models, along with associated software revisions for imaging enhancement.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company’s MRI systems are listed in the FDA’s 510(k) database, reflecting their regulatory compliance. Bruker Medical Imaging, Inc. is headquartered in the United States.
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
Bruker R28 Whole-Body Mr Scanner Ref K900026
510(k) 510(k)- 510(k) 510(k)
1989 Software Revision To The Bmt-1100 Ref K894714
510(k) 510(k)Magnetic Resonance System Model Bmt-1100 Ref K895328
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Bruker Medical Imaging, Inc. have in the registry?
The registry currently lists 7 devices for Bruker Medical Imaging, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bruker Medical Imaging, Inc.'s devices?
Among its 7 most recently registered devices, Bruker Medical Imaging, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Bruker Medical Imaging, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Bruker Medical Imaging, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bruker Medical Imaging, Inc. in the registry?
The most recently registered devices listed for Bruker Medical Imaging, Inc. include BRUKER R-28, HEAD AND CHEST ANGIOGRAPHY IMAGING ADD, MAGNETIC RESONANCE SYSTEM, MODEL BMT 1100, MODIFIED, BRUKER R28 WHOLE-BODY MR SCANNER and MODIFIED MAGNETIC RESONANCE IMAGING SYTEM MOD. R28.