The following data is part of a premarket notification filed by Suqian Ruijang Medical Supplies Co., Ltd with the FDA for Patient Examination Glove.
Device ID | K113193 |
510k Number | K113193 |
Device Name: | PATIENT EXAMINATION GLOVE |
Classification | Vinyl Patient Examination Glove |
Applicant | SUQIAN RUIJANG MEDICAL SUPPLIES CO., LTD 1 JIAN XIANG YUAN NO. 209 BEI SI HUAN ZHONG RD HAI DI Chu Xiaoan, CN 100083 |
Contact | Chu Xiaoan |
Correspondent | Chu Xiaoan SUQIAN RUIJANG MEDICAL SUPPLIES CO., LTD 1 JIAN XIANG YUAN NO. 209 BEI SI HUAN ZHONG RD HAI DI Chu Xiaoan, 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 | 2011-10-31 |
Decision Date | 2011-12-16 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00699320334706 | K113193 | 000 |