510(k) · Cleared

Cleared

Micro-Touch Nitrile

K093523510(k) AbbreviatedCleared Mar 4, 2010111-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

Ansell Healthcare Products, LLC · LZA Polymer Patient Examination Glove

Cleared on Mar 4, 2010 as substantially equivalent to K031580 (Green Prospect Sdn Bhd, 2003) after a 111-day review. Its family tree reaches back 1 generation to 2003.

Decided: Mar 4, 2010
Review: 111 days
Class: Class I
Product code: LZA
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K031580 (2003). No later device cites it as a predicate yet.

By dateBy generation

Root · 1 generation backK031580 Non-Sterile, Powder-Free, Blue Color Nitrile Examination GloveGreen Prospect Sdn Bhd · 2003
This deviceK093523 Micro-Touch NitrileAnsell Healthcare Products, LLC · 2010

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K031580	Non-Sterile, Powder-Free, Blue Color Nitrile Examination Glove	Green Prospect Sdn Bhd	2003	—
0 (this device)	K093523	Micro-Touch Nitrile	Ansell Healthcare Products, LLC	2010	—

FIG. 1 — Lineage of K093523, 2003–2010Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 LZA? 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 LZA device

#1 K192333 Blue Nitrile Examination Gloves Powder Freescore 71.0 · 2 generations · no Class I recall
#2 Held for the reportin the report
#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.

Type	Number	Device	Applicant	Decided	Recalls
*	K031580	Non-Sterile, Powder-Free, Blue Color Nitrile Examination Glove Summary page 1 …5) Legally Marketed Device to Which Equivalency is being Claimed: Device Name: Non-Sterile Powder-Free Blue Color Nitrile Examination Gloves 510(k) Number: K03 1580 6) Identification of the Device: Micro-Touch® Nitrice Powder-Free Blue Examination Gloves, Tested for Use with Chem…	Green Prospect Sdn Bhd	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 LZA devices

LZA Polymer Patient Examination Glove: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · LZA

24in 2025

2007high 146 (2022) · low 18 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LZA

110in 2025

2007high 212 (2019) · low 89 (2024)2026

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

Recalls per year · LZA

3so far in 2026, the most since 2007

2007high 3 (2026) · low 0 (2007)2026

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

Adverse event reports per year · LZA

73in 2025

2007high 76 (2024) · low 2 (2008)2025

MAUDE reports naming product code LZA, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	21	95	0	7
2008	18	97	0	2
2009	28	112	0	12
2010	31	97	0	12
2011	26	122	0	9
2012	33	110	0	11
2013	20	130	0	10
2014	27	197	0	8
2015	20	112	1	12
2016	30	171	1	25
2017	44	124	0	4
2018	22	178	0	3
2019	25	212	0	21
2020	30	101	0	4
2021	139	111	0	20
2022	146	111	0	19
2023	62	92	0	24
2024	30	89	0	76
2025	24	110	0	73
2026	15	103	3	—

What is it indicated for?

This is a medical glove to be worn on the hands of health care and similar personnel to

prevent contamination between health care personnel and the patient's body, fluids, waste or

environment, and tested for use with chemotherapy drugs.

Chemotherapy Drug Permeation

(average breakthrough detection time in minutes) (ASTM D6978-05)

*Car.mustine 12.4

Cyclophosphamide >240

Doxorubicin Hydrochloride >240

Etoposide (Toposar) >240

5-Fluorouracil >240

Paclitaxel (Toxol) >240

*ThioTEPA 19.6

Cisplatin >240

Dacarbazine >240

*WARN4ING: Do not use with Carmustine or ThioTEPA.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K093523 · printed Nov 4, 2026

Cite this page

510(k) Report. “K093523: Micro-Touch Nitrile.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K093523

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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