510(k) K062526

BLUE POWDERED LATEX EXAMINATION GLOVES, NON-STERILE by Multisafe Sdn. Bhd. — Product Code LYY

K062526 is an FDA 510(k) premarket notification submitted by Multisafe Sdn. Bhd. for the device "BLUE POWDERED LATEX EXAMINATION GLOVES, NON-STERILE". The FDA issued a decision of Substantially Equivalent on Apr 13, 2007. The device falls under product code LYY (Latex Patient Examination Glove), a Class I device regulated under 21 CFR 880.6250. Multisafe Sdn. Bhd. has 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Apr 13, 2007
Date Received
Aug 28, 2006
Clearance Type
Traditional
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
510(k)

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.