510(k) Report

510(k) · Decided

Decided

Irrigation Tray

K896800510(k) TraditionalDecided May 24, 1990174-day reviewClass I21 CFR 880.6960

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

Westmark, Sterile Packing Systems, Inc. (Sps) · KYZ Syringe, Irrigating (Non Dental)

Cleared on May 24, 1990 after a 174-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
May 24, 1990
Review
174 days
Class
Class I
Product code
KYZ
Recalls
None
Predicates
0

FDA has not posted a summary or statement for it, so its predicates are not known.

FIG. 1 — Lineage of K896800Source: FDA 510(k) database · 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KYZ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

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.

How does its category compare?

All KYZ devices

KYZ Syringe, Irrigating (Non Dental): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KYZ

1in 2020

2009: 12011: 12020: 1
2007high 1 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KYZ

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

Recalls per year · KYZ

1in 2023

2009: 12010: 22011: 12016: 52018: 12023: 1, 1 Class I2026 (partial year): 1
2007high 5 (2016) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · KYZ

28in 2025

2008: 42009: 32010: 22011: 42012: 12013: 122014: 102015: 112016: 82017: 522018: 762019: 692020: 882021: 412022: 112023: 142024: 1062025: 28
2007high 106 (2024) · low 0 (2007)2025

MAUDE reports naming product code KYZ, 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
20080—04
20091—13
20100—22
20111—14
20120—01
20130—012
20140—010
20150—011
20160—58
20170—052
20180—176
20190—069
20201—088
20210—041
20220—011
20230—1 (1)14
20240—0106
20250—028
20260—1—
Cite this page

510(k) Report. “K896800: Irrigation Tray.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K896800

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Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026