510(k) Report

510(k) · Cleared

Cleared

Hansen Medical Magellan Robotic Catheter 6Fr and Accessory Components

K151463510(k) SpecialCleared Aug 18, 201578-day reviewClass II21 CFR 870.1280

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Hansen Medical, Inc. · DRA Catheter, Steerable

Cleared on Aug 18, 2015 as substantially equivalent to K133552 (Hansen Medical, 2014) after a 78-day review. Its family tree reaches back 11 generations to 1990. 1 later device descends from it.

Decided
Aug 18, 2015
Review
78 days
Class
Class II
Product code
DRA
Recalls
None
Predicates
1

Its longest line of descent runs back 11 generations to K900765 (1990). 17 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by generationDescendants, by generation 4 generations back: 1 other ancestor5 generations back: 1 other ancestor6 generations back: 1 other ancestor7 generations back: 1 other ancestor11 generations back: 2 other ancestors 1 generation forward: 1 descendant K133552 · Magellan Robotic Catheter 6FR (Guide and Leader), Magellan Robotic Catheter 6FR Accessory Kit · Hansen Medical · 2014K132369 · Magellan Robotic System, Magellan Robotic Catheter 9FR · Hansen Medical, Inc. · 2013 · recalledK111004 · Hansen Medical Vascular Catheter Control System and Catheter · Hansen Medical, Inc. · 2012 · recalledK102168 · Sensei X Robotic Catheter System · Hansen Medical, Inc. · 2010 · recalledK091808 · Sensei Robotic Catheter System, Model 02057 · Hansen Medical, Inc. · 2009 · recalledK090365 · Hansen Medical Artisan S Control Catheter · Hansen Medical, Inc. · 2009 · recalledK073225 · Sensei Catheter Control System · Hansen Medical, Inc. · 2008 · recalledK052480 · Hansen Medical Catheter Control System (CCS) and Accessories, Hansen Medical Steerable Guide Catheter (SGC) and Sheath · Hansen Medical, Inc. · 2007 · recalledK021555 · Stereotaxis Niobe Magnetic Navigation System · Stereotaxis, Inc. · 2003K013484 · Telstar Magnetic Navigation Systems [MNS}, Telstar BI-Plane Digital Imaging System, Niobe Electrophysiology Mapping Cath · Stereotaxis, Inc. · 2002K900765 · Steerocath (TM) · Ep Technologies, Inc. · 1990−10−50
  1. Root · 11 generations backK900765 Steerocath (TM)Ep Technologies, Inc. · 1990
  2. 7 generations between
  3. 3 generations backK111004 Hansen Medical Vascular Catheter Control System and CatheterHansen Medical, Inc. · 2012 · Recalled
  4. 2 generations backK132369 Magellan Robotic System, Magellan Robotic Catheter 9FRHansen Medical, Inc. · 2013 · Recalled
  5. 1 generation backK133552 Magellan Robotic Catheter 6FR (Guide and Leader), Magellan Robotic…Hansen Medical · 2014
  6. This deviceK151463 Hansen Medical Magellan Robotic Catheter 6Fr and Accessory ComponentsHansen Medical, Inc. · 2015
  7. Descendant · cites it directly · 0 of its ownK153304 Hansen Medical Magellan Robotic Catheter eKitHansen Medical, Inc. · 2016
Show all 11 generations
  1. Root · 11 generations backK900765 Steerocath (TM)Ep Technologies, Inc. · 1990
  2. 10 generations backK013484 Telstar Magnetic Navigation Systems [MNS}, Telstar BI-Plane Digital…Stereotaxis, Inc. · 2002
  3. 9 generations backK021555 Stereotaxis Niobe Magnetic Navigation SystemStereotaxis, Inc. · 2003
  4. 8 generations backK052480 Hansen Medical Catheter Control System (CCS) and Accessories, Hansen…Hansen Medical, Inc. · 2007 · Recalled
  5. 7 generations backK073225 Sensei Catheter Control SystemHansen Medical, Inc. · 2008 · Recalled
  6. 6 generations backK090365 Hansen Medical Artisan S Control CatheterHansen Medical, Inc. · 2009 · Recalled
  7. 5 generations backK091808 Sensei Robotic Catheter System, Model 02057Hansen Medical, Inc. · 2009 · Recalled
  8. 4 generations backK102168 Sensei X Robotic Catheter SystemHansen Medical, Inc. · 2010 · Recalled
  9. 3 generations backK111004 Hansen Medical Vascular Catheter Control System and CatheterHansen Medical, Inc. · 2012 · Recalled
  10. 2 generations backK132369 Magellan Robotic System, Magellan Robotic Catheter 9FRHansen Medical, Inc. · 2013 · Recalled
  11. 1 generation backK133552 Magellan Robotic Catheter 6FR (Guide and Leader), Magellan Robotic…Hansen Medical · 2014
  12. This deviceK151463 Hansen Medical Magellan Robotic Catheter 6Fr and Accessory ComponentsHansen Medical, Inc. · 2015

Most influential descendants

Showing 1 of 1 · See all
  • K153304Hansen Medical Magellan Robotic Catheter eKitHansen Medical, Inc. · 2016 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K900765Steerocath (TM)Ep Technologies, Inc.1990—
−10K013484Telstar Magnetic Navigation Systems [MNS}, Telstar BI-Plane Digital Imaging…Stereotaxis, Inc.2002—
−9K021555Stereotaxis Niobe Magnetic Navigation SystemStereotaxis, Inc.2003—
−8K052480Hansen Medical Catheter Control System (CCS) and Accessories, Hansen Medical…Hansen Medical, Inc.20072
−7K073225Sensei Catheter Control SystemHansen Medical, Inc.20081
−6K090365Hansen Medical Artisan S Control CatheterHansen Medical, Inc.20091
−5K091808Sensei Robotic Catheter System, Model 02057Hansen Medical, Inc.20091
−4K102168Sensei X Robotic Catheter SystemHansen Medical, Inc.20101
−3K111004Hansen Medical Vascular Catheter Control System and CatheterHansen Medical, Inc.20122
−2K132369Magellan Robotic System, Magellan Robotic Catheter 9FRHansen Medical, Inc.20132
−1K133552Magellan Robotic Catheter 6FR (Guide and Leader), Magellan Robotic Catheter…Hansen Medical2014—
0 (this device)K151463Hansen Medical Magellan Robotic Catheter 6Fr and Accessory ComponentsHansen Medical, Inc.2015—
+1K153304Hansen Medical Magellan Robotic Catheter eKitHansen Medical, Inc.2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199320
199810
200110
200510
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
FIG. 1 — Lineage of K151463, 1990–2016Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in DRA? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new DRA device

  1. #1 K262165 FARADRIVE™ Steerable Sheath (M004PF21M402)score 13.2 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K133552Magellan Robotic Catheter 6FR (Guide and Leader), Magellan Robotic Catheter 6FR…
Summary page 4
…ansen Medical Magellan Robotic Catheter 6Fr v1.2 is substantially equivalent in intended use and method of operation to the Hansen Medical Magellan Robotic Catheter 6Fr (K133552). Hansen Medical Special 510(k) Submission Page 7-1 of 4 Magellan Robotic Catheter 6Fr v1.2…
Hansen Medical2014—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K153304Hansen Medical Magellan Robotic Catheter eKitHansen Medical, Inc.20160

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 25 years and passes through 4 companies; a new generation was cleared every 1.2 years on median.
  • 10 of the 17 ancestors have a recall of any class.
  • Of its descendants, K153304 (Hansen Medical, Inc., 2016) has gone furthest, with 0 descendants of its own.

How does its category compare?

All DRA devices

DRA Catheter, Steerable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · DRA

1in 2025

2007: 12008: 12009: 22010: 32011: 12012: 42014: 12015: 12016: 42017: 22018: 12019: 22020: 12021: 12022: 22023: 32025: 12026 (partial year): 1
2007high 4 (2012) · low 0 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DRA

89in 2023

2010: 29 days median2012: 70 days median2016: 123 days median2023: 89 days median
2007high 123 (2016) · low 29 (2010)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · DRA

4so far in 2026, the most since 2007

2008: 12011: 12026 (partial year): 4
2007high 4 (2026) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · DRA

4,018in 2025

2007: 62008: 232009: 52010: 22011: 1552012: 892013: 1132014: 2122015: 3502016: 4812017: 6252018: 6332019: 7002020: 7032021: 7412022: 6522023: 7882024: 1,9622025: 4,018
2007high 4,018 (2025) · low 2 (2010)2025

MAUDE reports naming product code DRA, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—06
20081—123
20092—05
201032902
20111—1155
2012470089
20130—0113
20141—0212
20151—0350
201641230481
20172—0625
20181—0633
20192—0700
20201—0703
20211—0741
20222—0652
20233890788
20240—01,962
20251—04,018
20261—4—

What is it indicated for?

The Hansen Medical Magellan Robotic Catheter 6Fr is intended to be used to

facilitate navigation to anatomical targets in the peripheral vasculature and

subsequently provide a conduit for manual placement of therapeutic devices.

The Magellan Robotic Catheter 6Fr is intended to be used with the Hansen

Medical Magellan Robotic System and accessories.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K151463: Hansen Medical Magellan Robotic Catheter 6Fr and Accessory Components.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151463

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026