510(k) K151390
K151390 is an FDA 510(k) premarket notification submitted by Maxter Glove Manufacturing Sdn Bhd for the device "Powder Free Nitrile Examination Gloves Tested For Use With Chemotherapy Drugs". The FDA issued a decision of Substantially Equivalent on May 2, 2016. The device falls under product code LZC (Medical Glove, Specialty), a Class I device regulated under 21 CFR 880.6250. Maxter Glove Manufacturing Sdn Bhd has 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 2, 2016
- Date Received
- May 26, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Medical Glove, Specialty
- Device Class
- Class I
- Regulation Number
- 880.6250
- Review Panel
- HO
- Submission Type
- 510(k)
A disposable medical glove (examination or surgeons) is a device that may or may not bear a trace amount of residual powder and is intended to be worn on the hand or finger(s) for medical purposes to prevent contamination. In addition, these gloves may have specialty claims such as chemotherapy, etc.