FDA 510(k) Application Details - K234097

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K234097
Device Name	Polymer Patient Examination Glove
Applicant	Ever Growth (Vietnam) Corporation Limited Long Khanh Industrial Zone, Binh Loc Commune, Long Khanh City 76461 VN Other 510(k) Applications for this Company
Contact	Deng Elizabeth 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	12/26/2023
Decision Date	03/27/2024
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