The following data is part of a premarket notification filed by Shen Wei (usa), Inc. with the FDA for Powder Free Latex Examination Gloves With Aloe Vera @ph 5.5 And Protein Labeling Claims.
| Device ID | K013793 |
| 510k Number | K013793 |
| Device Name: | POWDER FREE LATEX EXAMINATION GLOVES WITH ALOE VERA @PH 5.5 AND PROTEIN LABELING CLAIMS |
| Classification | Latex Patient Examination Glove |
| Applicant | SHEN WEI (USA), INC. 2845 WHIPPLE RD. Union City, CA 94587 |
| Contact | Belle L Chou |
| Correspondent | Belle L Chou SHEN WEI (USA), INC. 2845 WHIPPLE RD. Union City, CA 94587 |
| Product Code | LYY |
| CFR Regulation Number | 880.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-11-14 |
| Decision Date | 2002-01-22 |