FDA 510(k) Application Details - K212850

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K212850
Device Name	Polymer Patient Examination Glove
Applicant	Thai Rubber Industry Company Limited 738 Moo 5, Manam Koo Pluakdaeng 21140 TH Other 510(k) Applications for this Company
Contact	Supawadee Phoungthong 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	09/07/2021
Decision Date	12/10/2021
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