510(k) Report

510(k) · Cleared

Cleared

Ilt Deflecting Catheter, Model C114ND1

K010531510(k) SpecialCleared Apr 18, 200154-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

Intra Luminal Therapeutics, Inc. · DQY Catheter, Percutaneous

Cleared on Apr 18, 2001 after a 54-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 32 later devices descend from it.

Decided
Apr 18, 2001
Review
54 days
Class
Class II
Product code
DQY
Recalls
None
Predicates
0

32 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2002: 1 descendant cleared2003: 2 descendants cleared2008: 2 descendants cleared2004: 1 descendant cleared2015: 5 descendants cleared2006: 1 descendant cleared2014: 2 descendants cleared2011: 2 descendants cleared2012: 1 descendant cleared2019: 5 descendants cleared2013: 2 descendants cleared2016: 3 descendants cleared2024: 1 descendant cleared2017: 1 descendant cleared2018: 2 descendants cleared2023: 1 descendant cleared200020052010201520202025
  1. This deviceK010531 Ilt Deflecting Catheter, Model C114ND1Intra Luminal Therapeutics, Inc. · 2001
  2. Descendant · cites it directly · 30 of its ownK031692 Safe-Cross Deflecting Catheter, Model C114ND1Intra Luminal Therapeutics, Inc. · 2003
  3. Descendant · 2 generations on · 27 of its ownK032784 Ilt Safe-Cross Deflecting Catheter, Model C114ND1Intra Luminal Therapeutics, Inc. · 2003
  4. Descendant · 3 generations on · 26 of its ownK040481 Safe-Cross Deflecting Catheter, Model C118ND1Intra Luminal Therapeutics, Inc. · 2004
  5. Descendant · 4 generations on · 25 of its ownK062769 Pressurewire Certus, Models 12006 and 12306Radi Medical Systems AB · 2006
  6. Descendant · 5 generations on · 13 of its ownK080813 Pressurewire Certus, Certus (300CM), Aeris, Aeris (300CM), ReceiverRadi Medical Systems AB · 2008

Showing 5 of 32 descendants. See all descendants

Descendants cleared per year

2002: 12003: 22004: 12006: 12008: 22011: 22012: 12013: 22014: 22015: 52016: 32017: 12018: 22019: 52023: 12024: 1
2002high 5 (2015) · low 0 (2005)2026

Most influential descendants

Showing 5 of 32 · See all
  • K031692Safe-Cross Deflecting Catheter, Model C114ND1Intra Luminal Therapeutics, Inc. · 2003 · cites it directly30descendants
  • K032784Ilt Safe-Cross Deflecting Catheter, Model C114ND1Intra Luminal Therapeutics, Inc. · 2003 · 2 generations on27descendants
  • K040481Safe-Cross Deflecting Catheter, Model C118ND1Intra Luminal Therapeutics, Inc. · 2004 · 3 generations on26descendants
  • K062769Pressurewire Certus, Models 12006 and 12306Radi Medical Systems AB · 2006 · 4 generations on25descendants
  • K080813Pressurewire Certus, Certus (300CM), Aeris, Aeris (300CM), ReceiverRadi Medical Systems AB · 2008 · 5 generations on13descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K010531Ilt Deflecting Catheter, Model C114ND1Intra Luminal Therapeutics, Inc.2001—
+1K031692Safe-Cross Deflecting Catheter, Model C114ND1Intra Luminal Therapeutics, Inc.2003—
+2K032784Ilt Safe-Cross Deflecting Catheter, Model C114ND1Intra Luminal Therapeutics, Inc.2003—
+3K040481Safe-Cross Deflecting Catheter, Model C118ND1Intra Luminal Therapeutics, Inc.2004—
+4K062769Pressurewire Certus, Models 12006 and 12306Radi Medical Systems AB2006—
+5K080813Pressurewire Certus, Certus (300CM), Aeris, Aeris (300CM), ReceiverRadi Medical Systems AB2008—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
200320
200410
200610
200820
201120
201210
201320
201420
201550
201630
201710
201820
201950
202310
202410
FIG. 1 — Lineage of K010531, 2001–2024Source: 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), 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
Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (32)

See all 32

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K031692Safe-Cross Deflecting Catheter, Model C114ND1Intra Luminal Therapeutics, Inc.200330
K021638Ilt Advancing Mechanism, Model A115AMIIntra Luminal Therapeutics, Inc.20020

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?

  • Of its descendants, K031692 (Intra Luminal Therapeutics, Inc., 2003) has gone furthest, with 30 descendants of its own.

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)—

More from Intra Luminal Therapeutics, Inc.

20 FDA decisions under this applicant name. See the company

  • K050916Safe-Cross Radio Frequency Total Occlusion Crossing System [Peripheral]Intra Luminal Therapeutics, Inc. · 2005
  • K050915Safe-Cross Radio Frequency Total Occlusion Crossing System [Coronary]Intra Luminal Therapeutics, Inc. · 2005
  • K041973Modification to Safe-Cross Radio Frequency Total Occlusion Crossing SystemIntra Luminal Therapeutics, Inc. · 2004
  • K040481Safe-Cross Deflecting Catheter, Model C118ND1Intra Luminal Therapeutics, Inc. · 2004
  • K040037Modification to Safe-Cross Radio Frequency Total Occlusion Crossing SystemIntra Luminal Therapeutics, Inc. · 2004

Recent decisions in DQY

The DQY category page

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  • K260559NHanceITIMDS Operation B.V. · 2026
  • K262392APRO 35 Swift CatheterAlembic, LLC · 2026
  • K261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLC · 2026
  • K262240SSPC NXT Delivery CatheterCenterPoint Systems, LLC · 2026

https://510kreport.com/device/K010531 · printed Nov 6, 2026

Cite this page

510(k) Report. “K010531: Ilt Deflecting Catheter, Model C114ND1.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K010531

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026