510(k) Report

510(k) · Cleared

Cleared

Cantata Microcatheter

K101450510(k) SpecialCleared Dec 30, 2010220-day reviewClass II21 CFR 870.1210

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

Cook, Inc. · KRA Catheter, Continuous Flush

Cleared on Dec 30, 2010 as substantially equivalent to K060224 (Cook Incorporated, 2006) and 1 other predicate after a 220-day review. Its family tree reaches back 2 generations to 2006. 2 later devices descend from it.

Decided
Dec 30, 2010
Review
220 days
Class
Class II
Product code
KRA
Recalls
None
Predicates
2

Its longest line of descent runs back 2 generations to K060224 (2006). 2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2014: 1 descendant cleared2019: 1 descendant clearedK060224 · Modification to Mira-Flex 18 Microcatheter · Cook Incorporated · 2006K080737 · Miraflex High Flow Microcatheter · Cook, Inc. · 200820052010201520202025
Descendants, by generation 1 generation forward: 1 descendant2 generations forward: 1 descendant K080737 · Miraflex High Flow Microcatheter · Cook, Inc. · 2008K060224 · Modification to Mira-Flex 18 Microcatheter · Cook Incorporated · 20060
  1. Root · 2 generations backK060224 Modification to Mira-Flex 18 MicrocatheterCook Incorporated · 2006
  2. 1 generation backK080737 Miraflex High Flow MicrocatheterCook, Inc. · 2008
  3. This deviceK101450 Cantata MicrocatheterCook, Inc. · 2010
  4. Descendant · cites it directly · 1 of its ownK131772 Cantata (R) 2.9 MicrocatheterCook, Inc. · 2014
  5. Descendant · 2 generations on · 0 of its ownK191305 Hereaeus Poseidon MicrocatheterHeraeus Medical Components, LLC · 2019

Most influential descendants

Showing 2 of 2 · See all
  • K131772Cantata (R) 2.9 MicrocatheterCook, Inc. · 2014 · cites it directly1descendant
  • K191305Hereaeus Poseidon MicrocatheterHeraeus Medical Components, LLC · 2019 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K060224Modification to Mira-Flex 18 MicrocatheterCook Incorporated2006—
−1K080737Miraflex High Flow MicrocatheterCook, Inc.2008—
0 (this device)K101450Cantata MicrocatheterCook, Inc.2010—
+1K131772Cantata (R) 2.9 MicrocatheterCook, Inc.2014—
+2K191305Hereaeus Poseidon MicrocatheterHeraeus Medical Components, LLC2019—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
201910
FIG. 1 — Lineage of K101450, 2006–2019Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 KRA? 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 KRA device

  1. #1 K253509 TriSalus TriNav Advance Infusion Systemscore 14.4 · 9 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? (2)

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
*K060224Modification to Mira-Flex 18 Microcatheter
Summary page 1
…terms of intended use and technological characteristics and similar in terms of material with the predicate MiraFlex®18 Microcatheter cleared under 510(k) number K060224 and the MiraFlexa High Flow Microcatheter cleared under 510(k) number K(080737. The change involves a conversion from the cur…
Cook Incorporated2006—
*K080737Miraflex High Flow Microcatheter
Summary page 2
…equivalent tothe predicate MiraFlexl18 Microcatheter cleared under 510(k) number K060224 and MiraFlex® High Flow Microcatheter cleared under 510(k) number K080737. Test Data: '[he CantataM Microcatheter was subjected to the following tests to assure reliable design and p…
Cook, Inc.2008—

Also cleared against K060224: 2 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K131772Cantata (R) 2.9 MicrocatheterCook, Inc.20141

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 4 years and passes through 2 companies; a new generation was cleared every 2.4 years on median.
  • None of the 2 ancestors has a recall.
  • Of its descendants, K131772 (Cook, Inc., 2014) has gone furthest, with 1 descendant of its own.
  • 2 other devices also cite its predicate K060224.

How does its category compare?

All KRA devices

KRA Catheter, Continuous Flush: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · KRA

1in 2025

2007: 52008: 72009: 52010: 22011: 22012: 32013: 32014: 42016: 82017: 42018: 42019: 42020: 62021: 62022: 62023: 72025: 12026 (partial year): 5
2007high 8 (2016) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KRA

63in 2023

2007: 44 days median2008: 144 days median2009: 69 days median2012: 29 days median2013: 126 days median2014: 61 days median2016: 122 days median2017: 166 days median2018: 178 days median2019: 133 days median2020: 29 days median2021: 108 days median2022: 228 days median2023: 63 days median2026 (partial year): 268 days median
2007high 268 (2026) · low 29 (2012)2026

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

Recalls per year · KRA

41so far in 2026, the most since 2007

2007: 22008: 62009: 82010: 262011: 32012: 32013: 22014: 3, 2 Class I2015: 12016: 3, 1 Class I2019: 4, 4 Class I2020: 12023: 22026 (partial year): 41
2007high 41 (2026) · low 0 (2017)2026

Class I (7 since 2007) Class II/III not classified

Adverse event reports per year · KRA

980in 2025

2007: 1182008: 1172009: 1872010: 3552011: 2392012: 2172013: 2092014: 2762015: 3392016: 4182017: 5382018: 4342019: 4182020: 3812021: 4402022: 5432023: 8292024: 9422025: 980
2007high 980 (2025) · low 117 (2008)2025

MAUDE reports naming product code KRA, 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
20075442118
200871446117
20095698187
20102—26355
20112—3239
20123293217
201331262209
20144613 (2)276
20150—1339
201681223 (1)418
201741660538
201841780434
201941334 (4)418
20206291381
202161080440
202262280543
20237632829
20240—0942
20251—0980
2026526841—

What is it indicated for?

The Cantata™ Microcatheter is designed for use in small vessel or superselective anatomy for diagnostic and interventional procedures including neuro, peripheral, or coronary use.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K101450: Cantata Microcatheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K101450

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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