510(k) K240266
K240266 is an FDA 510(k) premarket notification submitted by Sri Trang Gloves (Thailand) Public Company Limited for the device "Latex Examination Glove Powder Free (Ocean Blue and Natural White)". The FDA issued a decision of Substantially Equivalent on September 9, 2024. The device falls under product code LYY (Latex Patient Examination Glove), a Class I device regulated under 21 CFR 880.6250. Sri Trang Gloves (Thailand) Public Company Limited has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 9, 2024
- Date Received
- January 31, 2024
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Latex Patient Examination Glove
- Device Class
- Class I
- Regulation Number
- 880.6250
- Review Panel
- HO
- Submission Type
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 potentially infectious materials and other contaminants.