Sgmp Co., Ltd. · Class I · Cleared Jun 12, 2003
| K-number | K030993 |
| Device name | NON-STERILE POWDERED GREEN COLORED POWDERED LATEX PATIENT EXAMINATION GLOVES WITH & WITHOUT SOUR/APPLE/PEPPERMINT SCENTS |
| Applicant | Sgmp Co., Ltd. |
| Product code | LYY |
| Device class | Class I |
| Decision date | Jun 12, 2003 |
| 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