The following data is part of a premarket notification filed by Inmed Corp. with the FDA for Celestin Dilator.
| Device ID | K812289 |
| 510k Number | K812289 |
| Device Name: | CELESTIN DILATOR |
| Classification | Dilator, Esophageal |
| Applicant | INMED CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KNQ |
| CFR Regulation Number | 876.5365 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-08-13 |
| Decision Date | 1981-09-01 |