| K-number | K933152 |
| Device name | MEROCEL MEROSPLINT |
| Applicant | Merocel Corp. |
| Product code | LYA |
| Device class | Class I |
| Decision date | Aug 17, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 874.4780 |
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