The following data is part of a premarket notification filed by Hebei Tengda Plastic Co., Ltd with the FDA for Powdered Vinyl Patient Examination Gloves.
| Device ID | K102151 |
| 510k Number | K102151 |
| Device Name: | POWDERED VINYL PATIENT EXAMINATION GLOVES |
| Classification | Vinyl Patient Examination Glove |
| Applicant | HEBEI TENGDA PLASTIC CO., LTD ROOM 1606 BLDG.1 JIANXIANG YUA NO.209 BEI SI HUAN ZHONG RD Shijiazhuang, CN 100083 |
| Contact | Chu Xiaoan |
| Correspondent | Chu Xiaoan HEBEI TENGDA PLASTIC CO., LTD ROOM 1606 BLDG.1 JIANXIANG YUA NO.209 BEI SI HUAN ZHONG RD Shijiazhuang, 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 | 2010-07-30 |
| Decision Date | 2011-04-27 |
| Summary: | summary |