510(k) Report

510(k) · Cleared

Cleared

Volcano S5I Intravascular Ultracound Imaging and Pressure System

K113486510(k) SpecialCleared Jan 27, 201265-day reviewClass II21 CFR 892.1560

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

Volcano Corporation · IYO System, Imaging, Pulsed Echo, Ultrasonic

Cleared on Jan 27, 2012 as substantially equivalent to K111706 (Volcano Corporation, 2011) after a 65-day review. Its family tree reaches back 8 generations to 1995. 2 later devices descend from it.

Decided
Jan 27, 2012
Review
65 days
Class
Class II
Product code
IYO
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K934139 (1995). 46 ancestors in all, the oldest K823434 (1982). 2 later devices descend from it, 1 citing it directly.

  1. Root · 8 generations backK934139 Tomtec Echo-ViewTomtec Tomographic Technologies GmbH · 1995
  2. 7 generations backK993398 Echo View, Easy View, Omni ViewTomtec Imaging Systems GmbH · 1999
  3. 6 generations backK022824 Echo-View 5.X, Easy-View 2.X, Omni View 2.X, Cardio-View 1.X, LV…Tomtec Imaging Systems GmbH · 2002
  4. 5 generations backK042188 Volcano Therapeutics, Inc. Volcano Ivus SystemVolcano Therapeutics, Inc. · 2004
  5. 4 generations backK051337 Eagle Eye Gold Ivus Imaging Catheter, Model 85900/859XX; Volcano…Volcano Corporation · 2005
  6. 3 generations backK071554 Volcano S5/S5I Intravascular Imaging and Pressure SystemVolcano Corporation · 2008 · Recalled
  7. 2 generations backK082229 S5/S5I Series Intravascular Imaging and Pressure System, Combomap…Volcano Corporation · 2008 · Recalled
  8. 1 generation backK111706 Volcano S5IINTRAVASCULAR Imaging and Pressure SystemVolcano Corporation · 2011 · Recalled
  9. This deviceK113486 Volcano S5I Intravascular Ultracound Imaging and Pressure SystemVolcano Corporation · 2012
  10. Descendant · cites it directly · 1 of its ownK122826 Preview Forward-Looking Ivus Catheter and Laptop System; Preview…Volcano Corporation · 2013
  11. Descendant · 2 generations on · 0 of its ownK132659 Volcano Preview Forward-Looking Ivus SystemVolcano Corporation · 2013

Most influential descendants

Showing 2 of 2 · See all
  • K122826Preview Forward-Looking Ivus Catheter and Laptop System; Preview Catheter Model 87000…Volcano Corporation · 2013 · cites it directly1descendant
  • K132659Volcano Preview Forward-Looking Ivus SystemVolcano Corporation · 2013 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K934139Tomtec Echo-ViewTomtec Tomographic Technologies GmbH1995—
−7K993398Echo View, Easy View, Omni ViewTomtec Imaging Systems GmbH1999—
−6K022824Echo-View 5.X, Easy-View 2.X, Omni View 2.X, Cardio-View 1.X, LV Analysis 1.X…Tomtec Imaging Systems GmbH2002—
−5K042188Volcano Therapeutics, Inc. Volcano Ivus SystemVolcano Therapeutics, Inc.2004—
−4K051337Eagle Eye Gold Ivus Imaging Catheter, Model 85900/859XX; Volcano VH-Ivus…Volcano Corporation2005—
−3K071554Volcano S5/S5I Intravascular Imaging and Pressure SystemVolcano Corporation20082
−2K082229S5/S5I Series Intravascular Imaging and Pressure System, Combomap Pressure and…Volcano Corporation20083
−1K111706Volcano S5IINTRAVASCULAR Imaging and Pressure SystemVolcano Corporation20111
0 (this device)K113486Volcano S5I Intravascular Ultracound Imaging and Pressure SystemVolcano Corporation2012—
+1K122826Preview Forward-Looking Ivus Catheter and Laptop System; Preview Catheter…Volcano Corporation2013—
+2K132659Volcano Preview Forward-Looking Ivus SystemVolcano Corporation2013—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
198610
199010
199110
199250
199330
199430
199520
199630
199730
199830
200020
200210
200320
200420
200530
200610
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201320
FIG. 1 — Lineage of K113486, 1995–2013Source: 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 IYO? 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 IYO device

  1. #1 K243937 Accuro 3Sscore 20.5 · 18 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? (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
*K111706Volcano S5IINTRAVASCULAR Imaging and Pressure System
Summary page 1
…ectrical Cable, 11, DSA PREDICATE DEVICE: Volcano s5 TM Intravascular Ultrasound Imaging System (K 111706) DEVICE DESCRIPTON: The modified Volcano s5 TM Intravascular Ultrasound Imaging and Pressure System is an integrated model, wi…
Volcano Corporation20111

Also cleared against K111706: 1 other device →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K122826Preview Forward-Looking Ivus Catheter and Laptop System; Preview Catheter Model 87000…Volcano Corporation20131

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 4 companies; a new generation was cleared every 2.4 years on median.
  • 5 of the 46 ancestors have a recall of any class.
  • Of its descendants, K122826 (Volcano Corporation, 2013) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K111706.

How does its category compare?

All IYO devices

IYO System, Imaging, Pulsed Echo, Ultrasonic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · IYO

7in 2025

2007: 202008: 142009: 132010: 152011: 112012: 152013: 172014: 142015: 192016: 102017: 192018: 142019: 132020: 112021: 152022: 52023: 112024: 102025: 72026 (partial year): 10
2007high 20 (2007) · low 5 (2022)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IYO

171in 2025

2007: 17 days median2008: 36 days median2009: 79 days median2010: 113 days median2011: 69 days median2012: 68 days median2013: 50 days median2014: 63 days median2015: 46 days median2016: 36 days median2017: 72 days median2018: 56 days median2019: 59 days median2020: 57 days median2021: 64 days median2022: 190 days median2023: 177 days median2024: 220 days median2025: 171 days median2026 (partial year): 139 days median
2007high 220 (2024) · low 17 (2007)2026

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

Recalls per year · IYO

1in 2022

2007: 42008: 52009: 92010: 82012: 22013: 32014: 22015: 12018: 12019: 12021: 112022: 12026 (partial year): 1
2007high 11 (2021) · low 0 (2011)2026

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

Adverse event reports per year · IYO

485in 2025

2007: 392008: 202009: 272010: 202011: 582012: 782013: 4362014: 3042015: 2682016: 2542017: 2382018: 3682019: 5372020: 4982021: 6172022: 5112023: 5272024: 6402025: 485
2007high 640 (2024) · low 20 (2008)2025

MAUDE reports naming product code IYO, 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
20072017439
20081436520
20091379927
201015113820
20111169058
20121568278
201317503436
201414632304
201519461268
201610360254
201719720238
201814561368
201913591537
202011570498
2021156411617
202251901511
2023111770527
2024102200640
202571710485
2026101391—

What is it indicated for?

The Volcano s5 TM Series Intravascular Imaging and Pressure System is used for the qualitative and quantitative evaluation of vascular morphology in the coronary arteries and vessels of the peripheral vasculature. It is also indicated as an adjunct to conventional angiographic procedures to provide an image of vessel lumen and wall structures. ChromaFlo® is indicated for qualitative blood flow information from peripheral and coronary vasculature; flow…

Read the full statement (227 words)

The Volcano s5 TM Series Intravascular Imaging and Pressure System is used for the qualitative and quantitative evaluation of vascular morphology in the coronary arteries and vessels of the peripheral vasculature. It is also indicated as an adjunct to conventional angiographic procedures to provide an image of vessel lumen and wall structures.

ChromaFlo® is indicated for qualitative blood flow information from peripheral and coronary vasculature; flow information can be an adjunct to other methods of estimating blood flow and blood perfusion.

VH® IVUS is intended to be used in conjunction with imaging catheters during diagnostic ultrasound imaging of the peripheral and coronary vasculature. The Volcano VH IVUS System is intended to semi: automatically visualize boundary features and perform spectra! analysis of RIF ultrasound signals of vascular features that the user may wish to examine more closely during routine diagnostic ultrasound imaging examinations.

The pressure feature is intended for use in all blood vessels, including coronary And peripheral arteries, to measure intravascular blood pressure during diagnostic angiography and/or interventional procedures.

Rotational 45MHz feature is intended for the qualitative and quantitative evaluation of vascular morphology in the coronary arteries and vasculature. As an adjunct to conventional angiographic procedures to provide an image of the vessel lumen and wall structures. The pullback feature of the PIMr withdraws the imaging core within the protective sheath for a maximum of 15 cm.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K113486: Volcano S5I Intravascular Ultracound Imaging and Pressure System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K113486

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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