The following data is part of a premarket notification filed by Wuxi Shenzhou Plastic Products Co., Ltd. with the FDA for Powdered Vinyl Patient Examination Gloves.
| Device ID | K070145 |
| 510k Number | K070145 |
| Device Name: | POWDERED 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 | 2007-02-28 |
| Summary: | summary |