510(k) K231973
K231973 is an FDA 510(k) premarket notification submitted by Ineo Tech Sdn Bhd for the device "PolyIsoprene Powder Free Black Colour Radiation Attenuating Surgical Glove". The FDA issued a decision of Substantially Equivalent on September 29, 2023. The device falls under product code KGO (Surgeon'S Gloves), a Class I device regulated under 21 CFR 878.4460.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 29, 2023
- Date Received
- July 3, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Surgeon'S Gloves
- Device Class
- Class I
- Regulation Number
- 878.4460
- Review Panel
- HO
- Submission Type
A surgeon's glove is a disposable device made of natural rubber latex or synthetic polymers that may or may not bear powder to facilitate donning, and it is intended to be worn on the hands, usually in surgical settings, to provide a barrier against potentially infectious materials and other contaminants.