510(k) · Cleared
ClearedPowder Free Latex Patient Examination Gloves, Tested for Use with Chemotherapy Drugs with a Protein Content Label Claim
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Wrp Asia Pacific Sdn. Bhd. · LZC Medical Glove, Specialty
Cleared on Jul 31, 2009 as substantially equivalent to K972616 (Wembley Rubber Products (M) Sdn Bhd, 1999) after a 255-day review. Its family tree reaches back 1 generation to 1999.
- Decided
- Jul 31, 2009
- Review
- 255 days
- Class
- Class I
- Product code
- LZC
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K972616 (1999). No later device cites it as a predicate yet.
- Root · 1 generation backK972616 Oncology Plus Powder Free Latex Examination Gloves (Protein Content…Wembley Rubber Products (M) Sdn Bhd · 1999
- This deviceK083410 Powder Free Latex Patient Examination Gloves, Tested for Use with…Wrp Asia Pacific Sdn. Bhd. · 2009
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K972616 | Oncology Plus Powder Free Latex Examination Gloves (Protein Content Labeling) | Wembley Rubber Products (M) Sdn Bhd | 1999 | — |
| 0 (this device) | K083410 | Powder Free Latex Patient Examination Gloves, Tested for Use with Chemotherapy… | Wrp Asia Pacific Sdn. Bhd. | 2009 | — |
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 LZC? 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 LZC device
- #1 K201390 Medline Powder-Free Light Blue Nitrile Exam…score 19.2 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
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 | Decided |
|---|---|---|---|
| * | K972616 | Oncology Plus Powder Free Latex Examination Gloves (Protein Content Labeling)Summary page 1…logy Plus Powder-Free Latex Examination Gloves (Protein Content Labeling, 50 micrograms or less) Regulatory Class I Product code: LYY 510(k): K972616 4.0 Description of The Device: Powder Free Latex Patient Examination Gloves, Tested for use with Chemotherapy… | 1999 |
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 LZC devicesLZC Medical Glove, Specialty: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.
FDA decisions per year · LZC
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LZC
85in 2022
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LZC
1in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LZC
10in 2025
MAUDE reports naming product code LZC, 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 | 1 | — | 0 | 0 |
| 2008 | 3 | 166 | 1 | 0 |
| 2009 | 5 | 253 | 0 | 1 |
| 2010 | 5 | 68 | 0 | 0 |
| 2011 | 0 | — | 4 | 1 |
| 2012 | 4 | 149 | 0 | 1 |
| 2013 | 0 | — | 0 | 1 |
| 2014 | 0 | — | 0 | 3 |
| 2015 | 1 | — | 0 | 0 |
| 2016 | 3 | 258 | 0 | 5 |
| 2017 | 6 | 121 | 0 | 7 |
| 2018 | 6 | 105 | 0 | 6 |
| 2019 | 7 | 200 | 0 | 8 |
| 2020 | 3 | 167 | 0 | 1 |
| 2021 | 3 | 94 | 1 | 2 |
| 2022 | 7 | 85 | 0 | 2 |
| 2023 | 0 | — | 0 | 1 |
| 2024 | 0 | — | 0 | 16 |
| 2025 | 1 | — | 0 | 10 |
| 2026 | 1 | — | 1 | — |
What is it indicated for?
The powder free chemotherapy examination glove is a specialty medical glove which is a disposable device intended for medical purposes that is worn on the examiner's hand or forefinger to prevent contamination between examiner and patient bodily fluids, waste or environment. Tested for use with chemotherapy drugs. Tested chemotherapy drugs are as follows [Cyclophosphamide, Carmustine, Thio-Tepa, Dacarbazine, Doxorubicin Hydrochloride; 5- Fluorouracil, Cisplatin, Etoposide, and Paclitaxel]
WARNING: DO NOT USE GLOVES WITH THIO-TEPA AND CARMUSTINE
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K083410 · printed Nov 5, 2026
Cite this page
510(k) Report. “K083410: Powder Free Latex Patient Examination Gloves, Tested for Use with Chemotherapy Drugs with a Protein Content Label Claim.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K083410
Report an extraction error
Are you the manufacturer?
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