Mirador Biomedical, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Mirador Biomedical, Inc. makes
Mirador Biomedical, Inc. manufactures medical devices for procedural access and pressure monitoring, including vascular access systems, lumbar puncture kits, intracranial pressure monitoring ports, and specialized pressure measurement tools for thoracic, abdominal, and compartmental applications. Their portfolio also includes CT-compatible access ports and assistive devices for epidural and arterial procedures.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. Mirador Biomedical, Inc. is based in the United States.
Catalogue
Compass Vascular Access; Compass Lumbar Puncture Ref K101518
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Compass Ct, Compass Ct Port Ref K133624
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mirador Biomedical, Inc. have in the registry?
The registry currently lists 4 devices for Mirador Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mirador Biomedical, Inc.'s devices?
Among its 4 most recently registered devices, Mirador Biomedical, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Mirador Biomedical, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Mirador Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mirador Biomedical, Inc. in the registry?
The most recently registered devices listed for Mirador Biomedical, Inc. include COMPASS VASCULAR ACCESS; COMPASS LUMBAR PUNCTURE, COMPASS VASCULAR ACCESS / ACCESS PORT / LUMBAR PUNCTURE / INTRACRANIAL PRESSURE, COMPASS CT, COMPASS CT PORT and COMPASS GLOBAL PRESSURE, COMPASS THORACENTESIS, PARACENTESIS, COMPARTMENT PRESSURE, EPIDURAL ASSIST, ARTERIAL ASSIST.