FDA 510(k) Application Details - K222693

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K222693
Device Name	Latex Patient Examination Glove
Applicant	Fitone Latex Products Co., Ltd. Guangdong No.5 Huitong road, Lingbei Industrial Zone, Suixi Zhanjiang 524338 CN Other 510(k) Applications for this Company
Contact	Christine Ou 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	09/06/2022
Decision Date	09/24/2022
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