Hong DI Plastic Products Co., Ltd. · Class I · Cleared Feb 13, 2007
| K-number | K070187 |
| Device name | POWDER FREE VINYL PATIENT EXAMINATION GLOVE |
| Applicant | Hong DI Plastic Products Co., Ltd. |
| Product code | LYZ |
| Device class | Class I |
| Decision date | Feb 13, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 880.6250 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov