The following data is part of a premarket notification filed by Wuxi Shenzhou Plastic Products Co., Ltd. with the FDA for Powder-free Vinyl Patient Examination Gloves.
Device ID | K070149 |
510k Number | K070149 |
Device Name: | POWDER-FREE VINYL PATIENT EXAMINATION GLOVES |
Classification | Vinyl Patient Examination Glove |
Applicant | WUXI SHENZHOU PLASTIC PRODUCTS CO., LTD. 209 BEI SI HUAN ZHONG RD, BD 1 ROOM 1606, JIANXIANG YUAN Haidian District, Beijing, CN 100083 |
Contact | Chu Xiaoan |
Correspondent | Chu Xiaoan WUXI SHENZHOU PLASTIC PRODUCTS CO., LTD. 209 BEI SI HUAN ZHONG RD, BD 1 ROOM 1606, JIANXIANG YUAN Haidian District, Beijing, CN 100083 |
Product Code | LYZ |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-01-16 |
Decision Date | 2007-02-23 |
Summary: | summary |