The following data is part of a premarket notification filed by Hebei Tengda Plastic Co., Ltd with the FDA for Powder-free Vinyl Patient Examination Gloves.
Device ID | K102152 |
510k Number | K102152 |
Device Name: | POWDER-FREE 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 | 2011-04-28 |
Summary: | summary |