510(k) K890459

JAMES RIVER BIOGEL POWDERLESS SURGICAL GLOVES by James River Corp. — Product Code KGO

K890459 is an FDA 510(k) premarket notification submitted by James River Corp. for the device "JAMES RIVER BIOGEL POWDERLESS SURGICAL GLOVES". The FDA issued a decision of Substantially Equivalent on April 20, 1989. The device falls under product code KGO (Surgeon'S Gloves), a Class I device regulated under 21 CFR 878.4460. James River Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 20, 1989
Date Received
January 30, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Surgeon'S Gloves
Device Class
Class I
Regulation Number
878.4460
Review Panel
HO
Submission Type

A surgeon's glove is a disposable device made of natural rubber latex or synthetic polymers that may or may not bear powder to facilitate donning, and it is intended to be worn on the hands, usually in surgical settings, to provide a barrier against potentially infectious materials and other contaminants.