FDA 510(k) Application Details - K212629

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K212629
Device Name	Polymer Patient Examination Glove
Applicant	EG Group Product and Services CO., Ltd 168/72 Nakniwat Road, Lat Phrao Bangkok 10230 TH Other 510(k) Applications for this Company
Contact	Aristotle Nafpliotis Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LZA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/19/2021
Decision Date	05/26/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review