| K-number | K931994 |
| Device name | RESECTOSCOPE SHEATH |
| Applicant | Olympus Corp. |
| Product code | HIH |
| Device class | Class II |
| Decision date | Feb 17, 1994 |
| Decision | Substantially Equivalent |
| Regulation | 884.1690 |
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