Joimax GmbH · Class II · Cleared Aug 12, 2005
| K-number | K051827 |
| Device name | JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS LAMINOSCOPE/MULTISCOPE |
| Applicant | Joimax GmbH |
| Product code | HRX |
| Device class | Class II |
| Decision date | Aug 12, 2005 |
| 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