510(k) Report

510(k) · Cleared

Cleared

Attain 6227DEF Deflectable Catheter Delivery System

K061480510(k) TraditionalCleared Aug 21, 200683-day reviewClass II21 CFR 870.1250

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

Medtronic, Ireland · DQY Catheter, Percutaneous

Cleared on Aug 21, 2006 as substantially equivalent to K032312 (Medtronic Vascular, 2003) after an 83-day review. Its family tree reaches back 5 generations to 1989.

Decided
Aug 21, 2006
Review
83 days
Class
Class II
Product code
DQY
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K893658 (1989). 37 ancestors in all, the oldest K770977 (1977). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2002: 1 other ancestor2001: 2 other ancestors1999: 2 other ancestors1996: 2 other ancestors1995: 3 other ancestors1994: 4 other ancestors1990: 5 other ancestors1993: 1 other ancestor1992: 3 other ancestors1991: 1 other ancestor1988: 1 other ancestor1987: 3 other ancestors1986: 1 other ancestor1985: 2 other ancestors1977: 1 other ancestorK893658 · Percutaneous Introducer · Medamicus, Inc. · 1989K965167 · Percutaneous Venous Introducer 10264 · Medamicus, Inc. · 1997K012130 · Attain LDS 6216 Left-Heart Delivery System · Medtronic Vascular · 2001K013517 · 10600 Deflectable Catheter System, Model 10600 · Medtronic Vascular · 2002K032312 · Attain 6226DEF Deflectable Catheter Delivery System · Medtronic Vascular · 20031975198019851990199520002005
  1. Root · 5 generations backK893658 Percutaneous IntroducerMedamicus, Inc. · 1989
  2. 4 generations backK965167 Percutaneous Venous Introducer 10264Medamicus, Inc. · 1997
  3. 3 generations backK012130 Attain LDS 6216 Left-Heart Delivery SystemMedtronic Vascular · 2001
  4. 2 generations backK013517 10600 Deflectable Catheter System, Model 10600Medtronic Vascular · 2002
  5. 1 generation backK032312 Attain 6226DEF Deflectable Catheter Delivery SystemMedtronic Vascular · 2003
  6. This deviceK061480 Attain 6227DEF Deflectable Catheter Delivery SystemMedtronic, Ireland · 2006
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K893658Percutaneous IntroducerMedamicus, Inc.1989—
−4K965167Percutaneous Venous Introducer 10264Medamicus, Inc.1997—
−3K012130Attain LDS 6216 Left-Heart Delivery SystemMedtronic Vascular2001—
−2K01351710600 Deflectable Catheter System, Model 10600Medtronic Vascular2002—
−1K032312Attain 6226DEF Deflectable Catheter Delivery SystemMedtronic Vascular2003—
0 (this device)K061480Attain 6227DEF Deflectable Catheter Delivery SystemMedtronic, Ireland2006—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197710
198520
198610
198730
198810
199050
199110
199230
199310
199440
199530
199620
199920
200120
200210
FIG. 1 — Lineage of K061480, 1989–2006Source: 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 DQY? 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 DQY device

  1. #1 K234115 APRO 55 Catheterscore 17.5 · 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
*K032312Attain 6226DEF Deflectable Catheter Delivery System
Summary page 2
…ses, function, materials and method of operation to the following predicate device: * Medtronic Attain 6226DEF Deflectable Catheter Delivery System (510(k) #032312, cleared November 3, 2003) Summary of Studies: Device integrity testing was performed to support the equivalency of the Attain®…
Medtronic Vascular2003—

Also cleared against K032312: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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 17 years and passes through 3 companies; a new generation was cleared every 2.8 years on median.
  • 5 of the 37 ancestors have a recall of any class.
  • 2 other devices also cite its predicate K032312.

How does its category compare?

All DQY devices

DQY Catheter, Percutaneous: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DQY

21in 2025

2007: 162008: 312009: 372010: 222011: 362012: 302013: 322014: 192015: 272016: 222017: 262018: 252019: 302020: 202021: 182022: 182023: 182024: 162025: 212026 (partial year): 11
2007high 37 (2009) · low 16 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DQY

115in 2025

2007: 85 days median2008: 66 days median2009: 73 days median2010: 74 days median2011: 71 days median2012: 87 days median2013: 92 days median2014: 127 days median2015: 118 days median2016: 117 days median2017: 113 days median2018: 106 days median2019: 111 days median2020: 120 days median2021: 81 days median2022: 74 days median2023: 114 days median2024: 87 days median2025: 115 days median2026 (partial year): 30 days median
2007high 127 (2014) · low 66 (2008)2026

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

Recalls per year · DQY

1in 2025

2007: 62008: 122009: 172010: 322011: 62012: 22013: 36, 1 Class I2014: 32015: 32016: 22, 7 Class I2017: 82018: 22019: 12020: 22021: 22023: 172024: 12025: 1, 1 Class I2026 (partial year): 2, 1 Class I
2007high 36 (2013) · low 0 (2022)2026

Class I (10 since 2007) Class II/III not classified

Adverse event reports per year · DQY

3,056in 2025

2007: 3132008: 4962009: 8192010: 1,2932011: 1,2112012: 1,1912013: 1,3522014: 1,4972015: 2,3372016: 2,2522017: 2,4892018: 2,8552019: 2,9022020: 2,8892021: 3,0062022: 2,6432023: 3,0492024: 3,1902025: 3,056
2007high 3,190 (2024) · low 313 (2007)2025

MAUDE reports naming product code DQY, 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
200716856313
2008316612496
2009377317819
20102274321,293
2011367161,211
2012308721,191
2013329236 (1)1,352
20141912731,497
20152711832,337
20162211722 (7)2,252
20172611382,489
20182510622,855
20193011112,902
20202012022,889
2021188123,006
2022187402,643
202318114173,049
2024168713,190
2025211151 (1)3,056
202611302 (1)—

What is it indicated for?

The deflectable catheter delivery system is indicated to provide a pathway though which diagnostic and therapeutic transvenous devices are introduced within the chambers and coronary vasculature of the heart, and for introducing balloon catheters into the coronary sinus or leads into vessels of the left heart via the coronary sinus.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K061480: Attain 6227DEF Deflectable Catheter Delivery System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K061480

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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