510(k) K083337

NUGARD, SENSIFLEX PROCEDURE EXAMINATION GLOVES by Terang Nusa Sdn Bhd — Product Code LYY

K083337 is an FDA 510(k) premarket notification submitted by Terang Nusa Sdn Bhd for the device "NUGARD, SENSIFLEX PROCEDURE EXAMINATION GLOVES". The FDA issued a decision of Substantially Equivalent on Jan 27, 2009. The device falls under product code LYY (Latex Patient Examination Glove), a Class I device regulated under 21 CFR 880.6250. Terang Nusa Sdn Bhd has 25 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Jan 27, 2009
Date Received
Nov 12, 2008
Clearance Type
Special
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.