The following data is part of a premarket notification filed by Shandong Junfeng Industries Co., Ltd with the FDA for Powder-free Vinyl Patient Examination Gloves, Clear (non-colored).
Device ID | K122266 |
510k Number | K122266 |
Device Name: | POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) |
Classification | Vinyl Patient Examination Glove |
Applicant | SHANDONG JUNFENG INDUSTRIES CO., LTD ROOM 1606 BLDG. 1. JIANXIANG YUAN BO. 209 BEI SI HUAN Beijing, CN 100083 |
Contact | Chu Xiaoan |
Correspondent | Chu Xiaoan SHANDONG JUNFENG INDUSTRIES CO., LTD ROOM 1606 BLDG. 1. JIANXIANG YUAN BO. 209 BEI SI HUAN 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 | 2012-07-30 |
Decision Date | 2012-09-27 |
Summary: | summary |