510(k) Report

510(k) · Cleared

Cleared

Strome-Blitzer Cytology Balloon

K182159510(k) TraditionalCleared Jun 13, 2019308-day reviewClass II21 CFR 874.4710

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

Adn International, LLC · EOX Esophagoscope (Flexible Or Rigid)

Cleared on Jun 13, 2019 as substantially equivalent to K911588 (Wilson-Cook Medical, Inc., 1992) after a 308-day review. Its family tree reaches back 1 generation to 1992.

Decided
Jun 13, 2019
Review
308 days
Class
Class II
Product code
EOX
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K911588 (1992). No later device cites it as a predicate yet.

  1. Root · 1 generation backK911588 Brandt Esophageal Cytology BalloonWilson-Cook Medical, Inc. · 1992
  2. This deviceK182159 Strome-Blitzer Cytology BalloonAdn International, LLC · 2019
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K911588Brandt Esophageal Cytology BalloonWilson-Cook Medical, Inc.1992—
0 (this device)K182159Strome-Blitzer Cytology BalloonAdn International, LLC2019—
FIG. 1 — Lineage of K182159, 1992–2019Source: 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 EOX? 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 EOX device

  1. #1 K222366 EsoCheck Cell Collection Devicescore 7.8 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K911588Brandt Esophageal Cytology Balloon
Summary page 4
…r FDA Document Numbers: None Basis of Submission: Traditional 510(k) based on K911588 (predicate device), K103437 (reference device) Number of Devices in Subm…
Wilson-Cook Medical, Inc.1992—
†K103437US Endoscopy Cytology BrushUnited States Endoscopy Group, Inc.20101

Also cleared against K911588: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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?

  • Its one ancestor has no recall.
  • 1 other device also cites its predicate K911588.

How does its category compare?

All EOX devices

EOX Esophagoscope (Flexible Or Rigid): FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · EOX

1in 2024

2007: 22011: 12012: 12013: 12014: 12016: 12018: 22019: 22020: 12021: 22022: 22023: 12024: 1
2007high 2 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EOX

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

Recalls per year · EOX

2in 2011

2011: 2
2007high 2 (2011) · low 0 (2007)2026

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

Adverse event reports per year · EOX

2in 2024

2009: 12010: 12012: 12015: 12016: 32017: 12020: 22022: 12023: 122024: 2
2007high 12 (2023) · low 0 (2007)2025

MAUDE reports naming product code EOX, 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
20072—00
20080—00
20090—01
20100—01
20111—20
20121—01
20131—00
20141—00
20150—01
20161—03
20170—01
20182—00
20192—00
20201—02
20212—00
20222—01
20231—012
20241—02
20250—00
20260—0—

What is it indicated for?

The Strome-Blitzer Cytology Balloon device is indicated for use in the 4-quadrant collection and retrieval of surface cells from the esophagus in adults (22 years of age or older). The device may be delivered transorally under direct endoscopic visualization.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K182159: Strome-Blitzer Cytology Balloon.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K182159

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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