Pentax Medical Company · Class II · Cleared Apr 9, 2014
| K-number | K131855 |
| Device name | PENTAX VIDEO COLONOSCOPES (EC FAMILY) |
| Applicant | Pentax Medical Company |
| Product code | FDF |
| Device class | Class II |
| Decision date | Apr 9, 2014 |
| 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