The following data is part of a premarket notification filed by Michael S. Upsher with the FDA for Upsher Fiberbrite Laryngoscope.
| Device ID | K832650 |
| 510k Number | K832650 |
| Device Name: | UPSHER FIBERBRITE LARYNGOSCOPE |
| Classification | Laryngoscope, Rigid |
| Applicant | MICHAEL S. UPSHER 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CCW |
| CFR Regulation Number | 868.5540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-08 |
| Decision Date | 1983-09-12 |