The following data is part of a premarket notification filed by Ever Light Plastic Products Co., Ltd. with the FDA for Ever Light Plastic Products Co., Ltd. Powder Free (white) Vinyl Patient Examination Gloves.
Device ID | K063213 |
510k Number | K063213 |
Device Name: | EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDER FREE (WHITE) VINYL PATIENT EXAMINATION GLOVES |
Classification | Vinyl Patient Examination Glove |
Applicant | EVER LIGHT PLASTIC PRODUCTS CO., LTD. 3973 SCHAEFER AVE Chino, CA 91710 |
Contact | Kathy Liu |
Correspondent | Kathy Liu EVER LIGHT PLASTIC PRODUCTS CO., LTD. 3973 SCHAEFER AVE Chino, CA 91710 |
Product Code | LYZ |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-10-23 |
Decision Date | 2006-12-05 |
Summary: | summary |