510(k) K182948

Gammex PI Hybrid Surgical Gloves Tested for Use with Chemotherapy Drugs by Ansell Healthcare Products, LLC — Product Code KGO

K182948 is an FDA 510(k) premarket notification submitted by Ansell Healthcare Products, LLC for the device "Gammex PI Hybrid Surgical Gloves Tested for Use with Chemotherapy Drugs". The FDA issued a decision of Substantially Equivalent on March 22, 2019. The device falls under product code KGO (Surgeon'S Gloves), a Class I device regulated under 21 CFR 878.4460. Ansell Healthcare Products, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 22, 2019
Date Received
October 23, 2018
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.