510(k) Report

510(k) · Cleared

Cleared

Tao Brush I.U.M.C. Endometrial Sampler

K170603510(k) TraditionalCleared May 24, 201784-day reviewClass II21 CFR 884.1100

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

Cook Incorporated · HFE Brush, Endometrial

Cleared on May 24, 2017 as substantially equivalent to K082066 (Cook Urological, Inc., 2008) after an 84-day review. Its family tree reaches back 2 generations to 1988. 1 later device descends from it.

Decided
May 24, 2017
Review
84 days
Class
Class II
Product code
HFE
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K881456 (1988). 3 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1995: 1 other ancestor2024: 1 descendant clearedK881456 · Pipelle DE Cornier Endometrial Suction Curette · Laboratoire Ccd C/O Washington Regulatory Services · 1988K082066 · Tao Brush I.U.M.C. Endometrial Sampler · Cook Urological, Inc. · 2008 · recalled1990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor 1 generation forward: 1 descendant K082066 · Tao Brush I.U.M.C. Endometrial Sampler · Cook Urological, Inc. · 2008 · recalledK881456 · Pipelle DE Cornier Endometrial Suction Curette · Laboratoire Ccd C/O Washington Regulatory Services · 19880
  1. Root · 2 generations backK881456 Pipelle DE Cornier Endometrial Suction CuretteLaboratoire Ccd C/O Washington Regulatory Services · 1988
  2. 1 generation backK082066 Tao Brush I.U.M.C. Endometrial SamplerCook Urological, Inc. · 2008 · Recalled
  3. This deviceK170603 Tao Brush I.U.M.C. Endometrial SamplerCook Incorporated · 2017
  4. Descendant · cites it directly · 0 of its ownK240595 Utepreva Endometrial Sampler (UP01)Utepreva, LLC · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K240595Utepreva Endometrial Sampler (UP01)Utepreva, LLC · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K881456Pipelle DE Cornier Endometrial Suction CuretteLaboratoire Ccd C/O Washington Regulatory Services1988—
−1K082066Tao Brush I.U.M.C. Endometrial SamplerCook Urological, Inc.20081
0 (this device)K170603Tao Brush I.U.M.C. Endometrial SamplerCook Incorporated2017—
+1K240595Utepreva Endometrial Sampler (UP01)Utepreva, LLC2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K170603, 1988–2024Source: 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), 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 HFE? 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 HFE device

  1. #1 K240595 Utepreva Endometrial Sampler (UP01)score 8.4 · 3 generations · no Class I recall
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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
*K082066Tao Brush I.U.M.C. Endometrial Sampler
Summary page 4
…rial Brush Classification Panel: Obstetrics/Gynecology Predicate Devices: The predicate device is the Tao Brush™ I.U.M.C. Endometrial Sampler cleared under 510(k) K082066. Device Description: The Tao Brush™ I.U.M.C. Endometrial Sampler has a working length of 26.9 centimeters and a 9.3 French oute…
Cook Urological, Inc.20081

Also cleared against K082066: 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
K240595Utepreva Endometrial Sampler (UP01)Utepreva, LLC20240

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 29 years and passes through 3 companies; a new generation was cleared every 20.1 years on median.
  • 2 of the 3 ancestors have a recall of any class.
  • Of its descendants, K240595 (Utepreva, LLC, 2024) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K082066.

How does its category compare?

All HFE devices

HFE Brush, Endometrial: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · HFE

1in 2024

2008: 12012: 12017: 12024: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HFE

Too few HFE 510(k)s in any year since 2007 to give a median.

Recalls per year · HFE

1in 2009

2009: 1
2007high 1 (2009) · low 0 (2007)2026

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

Adverse event reports per year · HFE

1in 2016

2009: 12012: 12016: 1
2007high 1 (2009) · low 0 (2007)2025

MAUDE reports naming product code HFE, 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
20070—00
20081—00
20090—11
20100—00
20110—00
20121—01
20130—00
20140—00
20150—00
20160—01
20171—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20241—00
20250—00
20260—0—

What is it indicated for?

The Tao Brush™ I.U.M.C. Endometrial Sampler is used to obtain endometrial cytological and histological samples.

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. “K170603: Tao Brush I.U.M.C. Endometrial Sampler.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K170603

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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