Atlas FDA

EKOS Corporation

8 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch EKOS Corporation

RecordFirmDate
The EKOS cart has the catalog number 700-60101. The EKOS cart is a custom infusion stand/c recall (Z-2890-2016)EKOS Corporation2016-09-27
EkoSonic Endovascular System, Catalog Number 500-56112. It consists of three main componen recall (Z-0864-2016)EKOS Corporation2016-02-24
The EKOS EkoSonic Control Unit is intended exclusively for use with the EkoSonic Endovascu recall (Z-2148-2015)EKOS Corporation2015-07-20
The EkoSonic Endovascular System employs high frequency (2-2.5 MHz), low power (0.585 watt recall (Z-0133-2014)EKOS Corporation2013-11-01
EkoSonic MACH4 Endovascular Device (Catalog #500-55106, 500-55112; 500-55118; 500-55124; 5 recall (Z-2023-2012)EKOS Corporation2012-07-17
EKOS EndoWave Infusion System consisting of a Drug Delivery Catheter and an Ultrasound Cor recall (Z-1892-2008)EKOS Corporation2008-09-16
PT-3B Control Unit - component of the EndoWave Infusion Catheter System. EndoWave Infusion recall (Z-1752-2008)EKOS Corporation2008-09-02
Infusion System. EKOS EndoWave Infusion System. EKOS EndoWave Infusion System Drug Deliver recall (Z-1773-2008)EKOS Corporation2008-08-20

Track EKOS Corporation automatically

Every clearance here is in the API, with alerts when new ones post.