Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

DXX — Predicate Candidate Screening

33 FDA 510(k) clearances under this product code; the 50 most recent screened below.

128 daysmedian FDA review time
283 days90th percentile
33clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K251792Stereotaxis GenesisX RMN with Navigant ™ Workstation (NWS)Stereotaxis, Inc.2025-11-061480
K243789LIBERTY Endovascular Robotic System (LIBERTYOS)Microbot Medical , Ltd.2025-09-042690
K221464CorPath GRX SystemCorindus, Inc.2022-07-27690
K202275CorPath GRX SystemCorindus, Inc.2020-12-111220
K180517CorPath GRX SystemCorindus, Inc.2018-03-29300
K173806CorPath GRX SystemCorindus, Inc.2018-03-01760
K173288CorPath GRX SystemCorindus, Inc.2018-02-151220
K160121CorPath GRX SystemCorindus, Inc.2016-10-272820
K152999CorPath 200 SystemCorindus, Inc.2016-03-181570
K150892CorPath 200 SystemCorindus, Inc.2015-10-021830
K151730Magellan Robotic SystemHansen Medical, Inc.2015-07-23270
K143227Magellan Robotic System, Magellan Robotic Catheter 10FrHansen Medical, Inc.2015-07-012330
K150312Vdrive system, Vdrive Duo, Vdrive with V-SonoStereotaxis, Inc.2015-06-171280
K141530VDRIVE SYSTEM/ VDRIVE DUO/ VDRIVE WITH V-CASStereotaxis, Inc.2014-12-181920
K140804VDRIVE WITH V-LOOP/ VDRIVE DUOStereotaxis, Inc.2014-09-031560
K141614MAGELLAN ROBOTIC SYSTEMHansen Medical2014-08-07521
K141822SENSEI X ROBOTIC CATHETER SYSTEMHanson Medical, Inc.2014-08-05291
K132369MAGELLAN ROBOTIC SYSTEM, MAGELLAN ROBOTIC CATHETER 9FRHansen Medical, Inc.2013-09-27591
K122488AMIGO REMOTE CATHETER SYSTEM & ACCESSORIESCatheter Robotics, Inc.2012-11-20970
K120834CORPATH 200 SYSTEMCorindus, Inc.2012-07-191220
K113628AMIGO REMOTE CATHETER SYSTEM (RCS) & ACCESSORIESCatheter Robotics, Inc.2012-06-121870
K111004HANSEN MEDICAL VASCULAR CATHETER CONTROL SYSTEM AND CATHETERHansen Medical, Inc.2012-05-294141
K102168SENSEI X ROBOTIC CATHETER SYSTEMHansen Medical, Inc.2010-10-22811
K091808SENSEI ROBOTIC CATHETER SYSTEM, MODEL 02057Hansen Medical, Inc.2009-09-10841
K090365HANSEN MEDICAL ARTISAN S CONTROL CATHETERHansen Medical, Inc.2009-05-07831
K073225SENSEI CATHETER CONTROL SYSTEMHansen Medical, Inc.2008-06-302281
K072371ODYSSEY WORKSTATIONStereotaxis, Inc.2007-11-14830
K052480HANSEN MEDICAL CATHETER CONTROL SYSTEM (CCS) AND ACCESSORIESHansen Medical, Inc.2007-05-026002
K051760NAVIGANT WORKSTATION WITH NIOBE MAGNETIC NAVIGATION SYSTEM, Stereotaxis, Inc.2006-05-053100
K032937NAVIGANT MAGNETIC NAVIGATION WORKSTATION 2.1 (NWS2) MODEL, 0Stereotaxis, Inc.2004-07-012830
K021555STEREOTAXIS NIOBE MAGNETIC NAVIGATION SYSTEMStereotaxis, Inc.2003-01-152470
K924125CRI ELECTRONIC CONTROL SYSTEMCatheter Research C/O Burditt, Bowles & Radzius1993-05-262820
K904787CRI STEERABLE CATHETER CONTROL SYSTEMCatheter Research C/O Burditt, Bowles & Radzius1990-12-17550

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda