The Olympus Optical Co. · Class II · Cleared Oct 22, 1998
| K-number | K982133 |
| Device name | OLYMPUS ENDOSCOPIC SYSTEM LUMBAR HERNIA DISCECTOMY AND ITS ANCILLARY EQUIPMENT |
| Applicant | The Olympus Optical Co. |
| Product code | HRX |
| Device class | Class II |
| Decision date | Oct 22, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 888.1100 |
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