Shinemound Enterprise, Inc. · Class I · Cleared Sep 30, 2005
| K-number | K051913 |
| Device name | POWDERED LATEX PATIENT EXAMINATION GLOVES |
| Applicant | Shinemound Enterprise, Inc. |
| Product code | LYY |
| Device class | Class I |
| Decision date | Sep 30, 2005 |
| 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