| K-number | K931792 |
| Device name | ARTHROSCOPE |
| Applicant | Intramed Laboratories, Inc. |
| Product code | HRH |
| Device class | Class I |
| Decision date | Jun 13, 1994 |
| Decision | Substantially Equivalent |
| Regulation | 886.4350 |
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