FDA 510(k) Application Details - K223304

Device Classification Name	Gown, Isolation, Surgical   More FDA Info for this Device
510(K) Number	K223304
Device Name	Gown, Isolation, Surgical
Applicant	Xiamen Probtain Medical Technology Co., Ltd 4th Floor, No.1 Building, No.6 Ji'an Road, Tong'an District Xiamen 361100 CN Other 510(k) Applications for this Company
Contact	Jianli Kang Other 510(k) Applications for this Contact
Regulation Number	878.4040   More FDA Info for this Regulation Number
Classification Product Code	FYC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/27/2022
Decision Date	02/08/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review