510(k) K990268

LAGLOVE BRAND POLYMER COATED LATEX EXAMINATION GLOVE (POWDER FREE) by La Glove (M) Sdn. Bhd. — Product Code LYY

K990268 is an FDA 510(k) premarket notification submitted by La Glove (M) Sdn. Bhd. for the device "LAGLOVE BRAND POLYMER COATED LATEX EXAMINATION GLOVE (POWDER FREE)". The FDA issued a decision of Substantially Equivalent on February 24, 1999. The device falls under product code LYY (Latex Patient Examination Glove), a Class I device regulated under 21 CFR 880.6250. La Glove (M) Sdn. Bhd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 24, 1999
Date Received
January 28, 1999
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

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.