| K-number | K812723 |
| Device name | PEARCE CORNEAL TREPHINE |
| Applicant | Visitec Co. |
| Product code | HRH |
| Device class | Class I |
| Decision date | Oct 13, 1981 |
| Decision | Substantially Equivalent |
| Regulation | 886.4350 |
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