The following data is part of a premarket notification filed by The Lebanon Corp. with the FDA for Relief Valve-honan Intraoc. Pressure.
| Device ID | K820526 |
| 510k Number | K820526 |
| Device Name: | RELIEF VALVE-HONAN INTRAOC. PRESSURE |
| Classification | Applicator, Ocular Pressure |
| Applicant | THE LEBANON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LCC |
| CFR Regulation Number | 886.4610 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-02-26 |
| Decision Date | 1982-03-25 |