The following data is part of a premarket notification filed by Zibo Yinghao Medical Products Co., Ltd with the FDA for Synthetic, Powder-free Nitrile Examination.
Device ID | K102593 |
510k Number | K102593 |
Device Name: | SYNTHETIC, POWDER-FREE NITRILE EXAMINATION |
Classification | Vinyl Patient Examination Glove |
Applicant | ZIBO YINGHAO MEDICAL PRODUCTS CO., LTD 12390 EAST END AVE Chino, CA 91710 |
Contact | Frank Liu |
Correspondent | Frank Liu ZIBO YINGHAO MEDICAL PRODUCTS CO., LTD 12390 EAST END 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 | 2010-09-09 |
Decision Date | 2010-12-20 |
Summary: | summary |