Tsi, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Tsi, Inc. makes
Tsi, Inc. manufactures blood perfusion monitors, including the Laserflo BPM403, BPM2, and modified variants such as the BPM403A. These devices measure tissue perfusion using laser Doppler technology, providing real-time data on blood flow in clinical settings.
The company’s blood perfusion monitors are classified as Class II devices under FDA regulations and are supported by 510(k) clearances. These devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Modified Laserflo Blood Perfusion Monitor Ref K864259
510(k) 510(k)Laserflo Blood Perfusion Monitor 403 Ref K851057
510(k) 510(k)Laserflo Blood Perfusion Monitor, Model BPM2 Ref K896515
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Tsi, Inc. have in the registry?
The registry currently lists 4 devices for Tsi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tsi, Inc.'s devices?
Among its 4 most recently registered devices, Tsi, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Tsi, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Tsi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tsi, Inc. in the registry?
The most recently registered devices listed for Tsi, Inc. include MODIFIED LASERFLO BLOOD PERFUSION MONITOR, LASERFLO BLOOD PERFUSION MONITOR 403, LASERFLO BLOOD PERFUSION MONITOR, MODEL BPM2 and MODIFIED LASERFLO BLOOD PERFUSION MONITOR, BPM403A.