510(k) · Cleared
ClearedDermasure Green Sterile SyntheticPolychloroprene Powder-Free Surgical Glove Tested for Use
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medline Industries, Inc. · KGO Surgeon'S Gloves
Cleared on Apr 1, 2020 after a 159-day review. FDA’s file for it is a 510(k) statement, which names no predicate.
- Decided
- Apr 1, 2020
- Review
- 159 days
- Class
- Class I
- Product code
- KGO
- Recalls
- None
- Predicates
- 0
FDA’s file for it is a 510(k) statement, which names no predicate.
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in KGO? 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 KGO device
- #1 K192328 JR.MEDIK Latex Surgeon’s Gloves Powder Freescore 15.2 · 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?
FDA’s file for it is a 510(k) statement, which names no predicate.
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 KGO devicesKGO Surgeon'S Gloves: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.
FDA decisions per year · KGO
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · KGO
185in 2023
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KGO
2in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KGO
21in 2025
MAUDE reports naming product code KGO, 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 | 10 | 113 | 0 | 13 |
| 2008 | 2 | — | 0 | 8 |
| 2009 | 3 | 48 | 15 | 14 |
| 2010 | 6 | 87 | 1 | 16 |
| 2011 | 11 | 90 | 0 | 14 |
| 2012 | 7 | 133 | 0 | 14 |
| 2013 | 6 | 184 | 0 | 41 |
| 2014 | 7 | 257 | 0 | 28 |
| 2015 | 12 | 225 | 0 | 11 |
| 2016 | 9 | 218 | 2 | 15 |
| 2017 | 12 | 111 | 1 | 20 |
| 2018 | 7 | 194 | 8 | 15 |
| 2019 | 11 | 204 | 0 | 51 |
| 2020 | 15 | 117 | 0 | 15 |
| 2021 | 14 | 199 | 0 | 14 |
| 2022 | 6 | 127 | 2 | 10 |
| 2023 | 14 | 185 | 2 | 28 |
| 2024 | 2 | — | 0 | 18 |
| 2025 | 1 | — | 0 | 21 |
| 2026 | 2 | — | 0 | — |
What is it indicated for?
This surgeon's glove is a device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination. In addition, these gloves were tested for use with chemotherapy drugs in accordance with ASTM D6978 Standard Practice for Assessment of Medical Gloves to Permeation by Chemotherapy Drugs. The following chemicals have been tested with these gloves. Chemotherapy Drug Permeation (Breakthrough Detection…
Read the full statement (223 words)
This surgeon's glove is a device made of synthetic rubber intended to be worn by operating room personnel to protect a surgical wound from contamination. In addition, these gloves were tested for use with chemotherapy drugs in accordance with ASTM D6978 Standard Practice for Assessment of Medical Gloves to Permeation by Chemotherapy Drugs.
The following chemicals have been tested with these gloves.
Chemotherapy Drug Permeation (Breakthrough Detection Time) in Minutes
Bleomycin (15 mg/ml) >240 minutes
Busulfan (6 mg/ml) >240 minutes
Carboplatin (10.0 mg/ml) >240 minutes
Carmustine (BCNU) (3.3 mg/ml) 38.5 minutes (57.2, 57.3, 38.5)
Cisplatin (1.0 mg/ml) >240 minutes
Cyclophosphamide (Cytoxan) (20 mg/ml) >240 minutes
Dacarbazine (DTIC) (10.0 mg/ml) >240 minutes
Doxorubicin Hydrochloride (2.0 mg/ml) >240 minutes
Epirubicin (Ellence) (2 mg/ml) >240 minutes
Etoposide (Toposar) (20.0 mg/ml) >240 minutes
Fludarabine (25.0 mg/ml) >240 minutes
Fluorouracil (50.0 mg/ml) >240 minutes
Idarubicin (1.0 mg/ml) >240 minutes
Ifosfamide (50.0 mg/ml) >240 minutes
Mechlorethamine HCI (1.0 mg/ml) >240 minutes
Melphalan (5 mg/ml) >240 minutes
Methotrexate (25 mg/ml) >240 minutes
Mitomycin C (0.5 mg/ml) >240 minutes
Mitoxantrone (2.0 mg/ml) >240 minutes
Paclitaxel (Taxol) (6.0 mg/ml) >240 minutes
Paraplatin (10 mg/ml) >240 minutes
Rituximab (10 mg/ml) >240 minutes
Thiotepa (10.0 mg/ml) 38.6 minutes (39.0, 39.3, 38.6)
Vincristine Sulfate (1.0 mg/ml) >240 minutes
Caution: Testing showed a minimum breakthrough time of 38.5 minutes for Carmustine and 38.6 minutes for Thiotepa.
Indications for use as stated in the FDA 510(k) statement.
https://510kreport.com/device/K192988 · printed Nov 6, 2026
Cite this page
510(k) Report. “K192988: Dermasure Green Sterile SyntheticPolychloroprene Powder-Free Surgical Glove Tested for Use.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192988
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Page last updated Nov 3, 2026