The following data is part of a premarket notification filed by Pentax Precision Instrument Corp. with the FDA for Broncho Fiberscope Fb-19c.
| Device ID | K832492 |
| 510k Number | K832492 |
| Device Name: | BRONCHO FIBERSCOPE FB-19C |
| Classification | Bronchoscope (flexible Or Rigid) |
| Applicant | PENTAX PRECISION INSTRUMENT CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EOQ |
| CFR Regulation Number | 874.4680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-07-27 |
| Decision Date | 1983-09-20 |