Brinkmann Instruments, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Brinkmann Instruments, Inc. makes
Brinkmann Instruments, Inc. manufactures precision capillaries designed for micromanipulation, enabling fine-scale control in laboratory and research applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Max L System Ref K761168
510(k) 510(k)Precision Capillaries For Micromanipulation Ref K024302
510(k) 510(k)
Frequently asked questions
How many devices does Brinkmann Instruments, Inc. have in the registry?
The registry currently lists 2 devices for Brinkmann Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brinkmann Instruments, Inc.'s devices?
Among its 2 most recently registered devices, Brinkmann Instruments, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Brinkmann Instruments, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Brinkmann Instruments, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brinkmann Instruments, Inc. in the registry?
The most recently registered devices listed for Brinkmann Instruments, Inc. include MAX L SYSTEM and PRECISION CAPILLARIES FOR MICROMANIPULATION.