The following data is part of a premarket notification filed by Jedmed Instrument Co. with the FDA for Entermed Entunit.
| Device ID | K802712 |
| 510k Number | K802712 |
| Device Name: | ENTERMED ENTUNIT |
| Classification | Unit, Examining/treatment, Ent |
| Applicant | JEDMED INSTRUMENT CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ETF |
| CFR Regulation Number | 874.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-10-31 |
| Decision Date | 1980-11-26 |