| K-number | K810095 |
| Device name | MOTI APRON |
| Applicant | Moti Enterprises, Inc. |
| Product code | KPY |
| Device class | Class I |
| Decision date | Feb 12, 1981 |
| Decision | Substantially Equivalent |
| Regulation | 892.6500 |
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