FDA 510(k) Application Details - K202377

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K202377
Device Name	Latex Patient Examination Glove
Applicant	Hi-Care Thai Gloves Co. Ltd. 199Moo.11, T. Banpru Hat Yai 90250 TH Other 510(k) Applications for this Company
Contact	Daniel John Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LYY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/20/2020
Decision Date	12/01/2020
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review