510(k) Report

510(k) · Cleared

Cleared

Sterile, Powder-Free, Latex Exam Gloves, Models 2D7018PF Series, 2D7028PF Series

K081464510(k) TraditionalCleared Aug 28, 200893-day reviewClass I21 CFR 880.6250

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

Cardinalhealth · LYY Latex Patient Examination Glove

Cleared on Aug 28, 2008 as substantially equivalent to K024292 (Allegiance Healthcare Corp., 2003) after a 93-day review. Its family tree reaches back 1 generation to 2003.

Decided
Aug 28, 2008
Review
93 days
Class
Class I
Product code
LYY
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K024292 (2003). No later device cites it as a predicate yet.

  1. Root · 1 generation backK024292 Modification to Positive Touch Powder-Free Latex Examination Gloves…Allegiance Healthcare Corp. · 2003
  2. This deviceK081464 Sterile, Powder-Free, Latex Exam Gloves, Models 2D7018PF Series…Cardinalhealth · 2008
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K024292Modification to Positive Touch Powder-Free Latex Examination Gloves with…Allegiance Healthcare Corp.2003—
0 (this device)K081464Sterile, Powder-Free, Latex Exam Gloves, Models 2D7018PF Series, 2D7028PF SeriesCardinalhealth2008—
FIG. 1 — Lineage of K081464, 2003–2008Source: 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 LYY? 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 LYY device

  1. #1 K202377 Palm Care Latex Examination Powder Free Glovesscore 12.7 · 2 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
*K024292Modification to Positive Touch Powder-Free Latex Examination Gloves with Protein and…
Summary page 1
…ove Classification: Glove, Exam LYY Predicate Devices: Cardinal Health's Powder-Free Latex Exam Gloves (K024292) Description: Latex Exam Gloves are formulated using Natural Rubber Latex. T…
Allegiance Healthcare Corp.2003—

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.

How does its category compare?

All LYY devices

LYY Latex Patient Examination Glove: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · LYY

1in 2025

2007: 122008: 132009: 72010: 132011: 112012: 112013: 62014: 32015: 32016: 42017: 42018: 22019: 12020: 12021: 82022: 142023: 22024: 12025: 1
2007high 14 (2022) · low 1 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LYY

150in 2022

2007: 75 days median2008: 151 days median2009: 76 days median2010: 106 days median2011: 127 days median2012: 133 days median2013: 131 days median2014: 156 days median2015: 251 days median2016: 142 days median2017: 230 days median2021: 188 days median2022: 150 days median
2007high 251 (2015) · low 75 (2007)2026

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

Recalls per year · LYY

1in 2020

2011: 12020: 1
2007high 1 (2011) · low 0 (2007)2026

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

Adverse event reports per year · LYY

1in 2025

2007: 112008: 142009: 112010: 102011: 42012: 12013: 22014: 62015: 52016: 72017: 72019: 72020: 12021: 12024: 62025: 1
2007high 14 (2008) · low 0 (2018)2025

MAUDE reports naming product code LYY, 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
20071275011
200813151014
2009776011
201013106010
20111112714
20121113301
2013613102
2014315606
2015325105
2016414207
2017423007
20182—00
20191—07
20201—11
2021818801
20221415000
20232—00
20241—06
20251—01
20260—0—

What is it indicated for?

A powder-free patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K081464: Sterile, Powder-Free, Latex Exam Gloves, Models 2D7018PF Series, 2D7028PF Series.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K081464

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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