The following data is part of a premarket notification filed by Shandong Aobo Medical Co, Ltd with the FDA for Powder Free Vinyl Patient Examination Gloves, Clear (non-colored).
Device ID | K092956 |
510k Number | K092956 |
Device Name: | POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) |
Classification | Vinyl Patient Examination Glove |
Applicant | SHANDONG AOBO MEDICAL CO, LTD ROOM 1066 BLDG, 1 JIAN XIANG YUAN NO 209 BEI SI HUAN ZHONG Road Hai Di, Beijing, CN 100083 |
Contact | Chu Xiaoan |
Correspondent | Chu Xiaoan SHANDONG AOBO MEDICAL CO, LTD ROOM 1066 BLDG, 1 JIAN XIANG YUAN NO 209 BEI SI HUAN ZHONG Road Hai Di, 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 | 2009-09-25 |
Decision Date | 2009-12-04 |
Summary: | summary |