| K-number | K003802 |
| Device name | HYSTEROSCOPES |
| Applicant | Global Endoscopy, Inc. |
| Product code | HIH |
| Device class | Class II |
| Decision date | Jul 22, 2001 |
| 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