Mirador Biomedical, Inc. is one of 13028 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mirador Biomedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: COMPASS GLOBAL PRESSURE, COMPASS THORACENTESIS, PARACENTESIS, COMPARTMENT PRESSURE, EPIDURAL ASSIST, ARTERIAL ASSIST, COMPASS VASCULAR ACCESS / ACCESS PORT / LUMBAR PUNCTURE / INTRACRANIAL PRESSURE
3
Total
3
Cleared
0
Denied
Mirador Biomedical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Seattle, US.
Historical record: 3 cleared submissions from 2010 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mirador Biomedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mirador Biomedical, Inc.
3 devices
Cleared
Dec 14, 2011
COMPASS GLOBAL PRESSURE, COMPASS THORACENTESIS, PARACENTESIS, COMPARTMENT...
Cardiovascular
135d
Cleared
Jan 20, 2011
COMPASS VASCULAR ACCESS / ACCESS PORT / LUMBAR PUNCTURE / INTRACRANIAL PRESSURE
Cardiovascular
30d
Cleared
Oct 13, 2010
COMPASS VASCULAR ACCESS
Cardiovascular
133d