The following data is part of a premarket notification filed by Shijiazhuang Manful Light Industrial Products Co., with the FDA for Powdered Vinyl Patient Examination Gloves.
Device ID | K042120 |
510k Number | K042120 |
Device Name: | POWDERED VINYL PATIENT EXAMINATION GLOVES |
Classification | Vinyl Patient Examination Glove |
Applicant | SHIJIAZHUANG MANFUL LIGHT INDUSTRIAL PRODUCTS CO., RM 707, AVIC BLDG, NO 2 DONG SAN HUAN NAN ROAD Chaoyang; Beijing, CN 10002 |
Contact | Chen Yuhong |
Correspondent | Chen Yuhong SHIJIAZHUANG MANFUL LIGHT INDUSTRIAL PRODUCTS CO., RM 707, AVIC BLDG, NO 2 DONG SAN HUAN NAN ROAD Chaoyang; Beijing, CN 10002 |
Product Code | LYZ |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-08-06 |
Decision Date | 2004-11-04 |
Summary: | summary |