FDA 510(k) Application Details - K220644

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K220644
Device Name	Polymer Patient Examination Glove
Applicant	YTY Industry (Manjung) Sdn Bhd Lot 1422-1424, Batu 10 Lekir Sitiawan 32020 MY Other 510(k) Applications for this Company
Contact	Punitha Samy 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	03/04/2022
Decision Date	03/25/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review