The following data is part of a premarket notification filed by Pentax Precision Instrument Corp. with the FDA for Pentax Fd-34a Duodenofiberscope.
| Device ID | K832006 |
| 510k Number | K832006 |
| Device Name: | PENTAX FD-34A DUODENOFIBERSCOPE |
| Classification | Duodenoscope And Accessories, Flexible/rigid |
| Applicant | PENTAX PRECISION INSTRUMENT CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FDT |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-23 |
| Decision Date | 1983-08-01 |