Powder-Free Black Latex Examination Gloves with Protein Labeling (50 Micrograms or Less of Total Water Extractable Prote
K060229 is the FDA 510(k) clearance record for POWDER-FREE BLACK LATEX EXAMINATION GLOVES WITH PROTEIN LABELING (50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTABLE PROTE, a class I device, cleared for Shun Thai Rubber Gloves Industry Public Co., Ltd. on under FDA product code LYY (Latex Patient Examination Glove). FDA's definition for product code LYY reads: "A latex patient examination glove is a disposable device made of natural rubber latex that may or may not bear a trace amount of residual powder, and is intended to be worn on the hand for medical purposes to provide a barrier against...". FDA records list 6 510(k) clearances for Shun Thai Rubber Gloves Industry Public Co., Ltd., from to . As of , FDA records show no recalls naming K060229.
Clearance record
- Decision date
- Received
- (44 days to decision)
- Product code
- LYY Latex Patient Examination Glove
- Regulation
- 21 CFR 880.6250
- Device class
- Class I
- Review panel
- General Hospital
- Applicant
- Shun Thai Rubber Gloves Industry Public Co., Ltd. 198 Ave. De La D'Emerald, Sparks NV
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code LYY
Trailing 12 monthsFDA records hold no clearances under product code LYY in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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