510(k) Report

510(k) · Cleared

Cleared

Kodak Dental Barrier Pac

K884827510(k) TraditionalCleared Jan 30, 198973-day reviewClass I21 CFR 892.1840

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

Eastman Kodak Company · IWZ Film, Radiographic

Cleared on Jan 30, 1989 after a 73-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jan 30, 1989
Review
73 days
Class
Class I
Product code
IWZ
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1998: 1 descendant cleared1990200020102020
  1. This deviceK884827 Kodak Dental Barrier PacEastman Kodak Company · 1989
  2. Descendant · cites it directly · 0 of its ownK980543 Denoptix Barrier Envelope (Size 0-4)Dentsply Intl. · 1998

Most influential descendants

Showing 1 of 1 · See all
  • K980543Denoptix Barrier Envelope (Size 0-4)Dentsply Intl. · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K884827Kodak Dental Barrier PacEastman Kodak Company1989—
+1K980543Denoptix Barrier Envelope (Size 0-4)Dentsply Intl.1998—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
FIG. 1 — Lineage of K884827, 1989–1998Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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  • 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? (1)

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

NumberDeviceApplicantDecidedDescendants
K980543Denoptix Barrier Envelope (Size 0-4)Dentsply Intl.19980

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?

  • Of its descendants, K980543 (Dentsply Intl., 1998) has gone furthest, with 0 descendants of its own.

How does its category compare?

All IWZ devices

IWZ Film, Radiographic: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · IWZ

FDA has decided no IWZ device since 2007.

Median 510(k) review, days · IWZ

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

Recalls per year · IWZ

1in 2019

2010: 32011: 22013: 12014: 12019: 1
2007high 3 (2010) · low 0 (2007)2026

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

Adverse event reports per year · IWZ

1in 2023

2008: 12009: 12018: 12023: 1
2007high 1 (2008) · low 0 (2007)2025

MAUDE reports naming product code IWZ, 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—01
20090—01
20100—30
20110—20
20120—00
20130—10
20140—10
20150—00
20160—00
20170—00
20180—01
20190—10
20200—00
20210—00
20220—00
20230—01
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K884827: Kodak Dental Barrier Pac.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K884827

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