510(k) Report

510(k) · Cleared

Cleared

Olympus MH-246R Balloon Sheath, for Bronchial Use

K982733510(k) TraditionalCleared Oct 28, 199884-day reviewClass II21 CFR 892.1570

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

The Olympus Optical Co. · ITX Transducer, Ultrasonic, Diagnostic

Cleared on Oct 28, 1998 as substantially equivalent to K961048 (Olympus America, Inc., 1996) after an 84-day review. Its family tree reaches back 2 generations to 1987. 1 later device descends from it.

Decided
Oct 28, 1998
Review
84 days
Class
Class II
Product code
ITX
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K872027 (1987). 4 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1993: 1 other ancestor1988: 1 other ancestor2000: 1 descendant clearedK872027 · Olympus GF-UM2/EU-M2 · Olympus Corp. · 1987K961048 · Olympus MH-246R Balloon Sheath · Olympus America, Inc. · 19961990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 2 other ancestors 1 generation forward: 1 descendant K961048 · Olympus MH-246R Balloon Sheath · Olympus America, Inc. · 1996K872027 · Olympus GF-UM2/EU-M2 · Olympus Corp. · 19870
  1. Root · 2 generations backK872027 Olympus GF-UM2/EU-M2Olympus Corp. · 1987
  2. 1 generation backK961048 Olympus MH-246R Balloon SheathOlympus America, Inc. · 1996
  3. This deviceK982733 Olympus MH-246R Balloon Sheath, for Bronchial UseThe Olympus Optical Co. · 1998
  4. Descendant · cites it directly · 0 of its ownK994106 Olympus UM-S30-25R Ultrasonic Probe and Associated Ancillary…Olympus America, Inc. · 2000

Most influential descendants

Showing 1 of 1 · See all
  • K994106Olympus UM-S30-25R Ultrasonic Probe and Associated Ancillary Equipment for Bronchial UseOlympus America, Inc. · 2000 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K872027Olympus GF-UM2/EU-M2Olympus Corp.1987—
−1K961048Olympus MH-246R Balloon SheathOlympus America, Inc.1996—
0 (this device)K982733Olympus MH-246R Balloon Sheath, for Bronchial UseThe Olympus Optical Co.1998—
+1K994106Olympus UM-S30-25R Ultrasonic Probe and Associated Ancillary Equipment for…Olympus America, Inc.2000—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
199310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200010
FIG. 1 — Lineage of K982733, 1987–2000Source: 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 ITX? 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 ITX device

  1. #1 K260114 Align® Cover and Pad Guidance Toolscore 13.6 · 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? (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
*K961048Olympus MH-246R Balloon Sheath
Summary page 1
…II, 21 CFR 892.1570, Diagnostic Ultrasound and Name: Transducer Class II, 21 CFR 874.4680 Bronchoscope and accessories Predicate Devices: Olympus MH-246R (for GI use), K961048 Submitted by: Laura Storms-Tyler Olympus America Inc. Regulatory Affairs Two Corporate Drive Melville, NY 11747-3157 phone (51…
Olympus America, Inc.1996—

Also cleared against K961048: 2 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K994106Olympus UM-S30-25R Ultrasonic Probe and Associated Ancillary Equipment for Bronchial UseOlympus America, Inc.20000

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 11 years and passes through 3 companies; a new generation was cleared every 9.1 years on median.
  • 1 of the 4 ancestors has a recall of any class.
  • Of its descendants, K994106 (Olympus America, Inc., 2000) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K961048.

How does its category compare?

All ITX devices

ITX Transducer, Ultrasonic, Diagnostic: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · ITX

4in 2025

2007: 102008: 122009: 172010: 102011: 102012: 72013: 32014: 42015: 12016: 42017: 62018: 22019: 12020: 32021: 32022: 22023: 62024: 32025: 42026 (partial year): 6
2007high 17 (2009) · low 1 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ITX

126in 2025

2007: 26 days median2008: 73 days median2009: 28 days median2010: 42 days median2011: 16 days median2012: 25 days median2013: 105 days median2014: 41 days median2016: 151 days median2017: 110 days median2020: 120 days median2021: 139 days median2023: 213 days median2024: 81 days median2025: 126 days median2026 (partial year): 158 days median
2007high 213 (2023) · low 16 (2011)2026

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

Recalls per year · ITX

2in 2025

2008: 42009: 42010: 42011: 12012: 12014: 12015: 52017: 12018: 152020: 32021: 10, 10 Class I2022: 62023: 12024: 12025: 2
2007high 15 (2018) · low 0 (2007)2026

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

Adverse event reports per year · ITX

571in 2025

2007: 162008: 392009: 232010: 302011: 342012: 292013: 382014: 432015: 1832016: 2692017: 4122018: 1302019: 1192020: 1162021: 1462022: 872023: 1382024: 9882025: 571
2007high 988 (2024) · low 16 (2007)2025

MAUDE reports naming product code ITX, 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
20071026016
20081273439
20091728423
20101042430
20111016134
2012725129
20133105038
2014441143
20151—5183
201641510269
201761101412
20182—15130
20191—0119
202031203116
2021313910 (10)146
20222—687
202362131138
20243811988
202541262571
202661580—

What is it indicated for?

Olympus MH-246R Balloon Sheath have been designed to be used with the Olympus Ultrasonic Probe UM-2R/UM-3R, for intraluminal ultrasonic imaging of the upper airways and the tracheobronchial tree.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K982733: Olympus MH-246R Balloon Sheath, for Bronchial Use.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K982733

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