FDA 510(k) Application Details - K221718

Device Classification Name	Surgeon'S Gloves   More FDA Info for this Device
510(K) Number	K221718
Device Name	Surgeon'S Gloves
Applicant	Hartalega NGC SDN BHD NO. 1, Persiaran Tanjung Kawasan Perindustrian Tanjung Sepang 43900 MY Other 510(k) Applications for this Company
Contact	Kuan Mun Leong Other 510(k) Applications for this Contact
Regulation Number	878.4460   More FDA Info for this Regulation Number
Classification Product Code	KGO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/13/2022
Decision Date	09/24/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review