FDA 510(k) Application Details - K243792

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K243792
Device Name	Polymer Patient Examination Glove
Applicant	Basic Medical Technology Inc. 5300 Concours Street Ontario, CA 91764 US Other 510(k) Applications for this Company
Contact	John Zhao 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	12/10/2024
Decision Date	02/18/2025
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