510(k) K220232
K220232 is an FDA 510(k) premarket notification submitted by Megine Industries Sdn Bhd for the device "Nitrile Powder Free Examination Gloves, Non-Sterile - Blue, Black, Orange". The FDA issued a decision of Substantially Equivalent on Feb 20, 2022. The device falls under product code LZA (Polymer Patient Examination Glove), a Class I device regulated under 21 CFR 880.6250. Megine Industries Sdn Bhd has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 20, 2022
- Date Received
- Jan 27, 2022
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Polymer Patient Examination Glove
- Device Class
- Class I
- Regulation Number
- 880.6250
- Review Panel
- HO
- Submission Type
- 510(k)
A nitrile (or polymer) patient examination glove is a disposable device made of nitrile rubber or synthetic polymers 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.