Vasamedics, LLC is one of 24547 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vasamedics, LLC - FDA 510(k) Cleared Devices
Recent clearances: VENTRICULAR CATHETER BLOOD FLOW MONITORING PROBE KIT AND VENTRAFLO BLOOD FLOW MONITORING PROBE KIT, TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT, LASERFLO BLOOD PERFUSION SINGLE USE PROBES MODELS SUP-440, SUPR-434 SUP-433
6
Total
5
Cleared
0
Denied
Vasamedics, LLC has 5 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 5 cleared submissions from 1991 to 1997. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vasamedics, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vasamedics, LLC
6 devices
Cleared
Apr 09, 1997
VENTRICULAR CATHETER BLOOD FLOW MONITORING PROBE KIT AND VENTRAFLO BLOOD FLOW...
Cardiovascular
271d
Cleared
Oct 11, 1996
TRIMFLO PARENCHYMAL BLOOD FLOW MONITORING PROBE KIT
Cardiovascular
185d
Cleared
Mar 21, 1996
LASERFLO BLOOD PERFUSION SINGLE USE PROBES MODELS SUP-440, SUPR-434 SUP-433
Cardiovascular
336d
Cleared
Jun 29, 1995
MODEL PV2000 VASCULAR MICROLABORATORY
Cardiovascular
91d
Cleared
Dec 12, 1991
MODIF. LASERFLO BLOOD PERFUSION MONITOR MODEL BPM2
Cardiovascular
192d
Cleared
Aug 13, 1991
LASERFLO(R) BLOOD PERFUSION MONITOR (MODEL BPM2)
Cardiovascular
116d