Olympus America, Inc. · Class II · Cleared Aug 27, 2001
| K-number | K011886 |
| Device name | OLYMPUS EU-M60 EUS EXERA ENDOSCOPIC ULTRASOUND CTR, EUS EXERA ULTRASONIC GASTROVIDEOSCOPE OLYMPUS GF TYPE UM 160, |
| Applicant | Olympus America, Inc. |
| Product code | ODG |
| Device class | Class II |
| Decision date | Aug 27, 2001 |
| Decision | Substantially Equivalent |
| Regulation | 876.1500 |
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