The following data is part of a premarket notification filed by Jiangxi Jiangxi Zhonghong Pulin Medical Products Co.,ltd. with the FDA for Nitrile Patient Examination Glove.
Device ID | K222534 |
510k Number | K222534 |
Device Name: | Nitrile Patient Examination Glove |
Classification | Polymer Patient Examination Glove |
Applicant | Jiangxi Jiangxi Zhonghong Pulin Medical Products Co.,Ltd. Yinshawan Park, High-tech Industrial Park, Hukou County Jiujiang, CN 332599 |
Contact | Zhou Ziyu |
Correspondent | Boyle Wang Shanghai Truthful Information Technology Co., Ltd. RM.608,No.738,Shangcheng Rd.,Pudong Shanghai, CN 200120 |
Product Code | LZA |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2022-08-22 |
Decision Date | 2022-11-23 |