Kelleher Corp. · Class I · Cleared Aug 12, 1982
| K-number | K822011 |
| Device name | SHEA'S EAR SPECULUM HOLDER PORT MANNS |
| Applicant | Kelleher Corp. |
| Product code | JYK |
| Device class | Class I |
| Decision date | Aug 12, 1982 |
| Decision | Substantially Equivalent |
| Regulation | 878.1800 |
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