Richard Wolf Medical Instruments Corp. · Class II · Cleared Dec 7, 1992
| K-number | K920235 |
| Device name | ULTRASOUND GENERATOR MODLE 2270 |
| Applicant | Richard Wolf Medical Instruments Corp. |
| Product code | FEO |
| Device class | Class II |
| Decision date | Dec 7, 1992 |
| Decision | Substantially Equivalent |
| Regulation | 876.4480 |
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