The following data is part of a premarket notification filed by Preat Corp. with the FDA for Endodontic Post Systems.
| Device ID | K810977 |
| 510k Number | K810977 |
| Device Name: | ENDODONTIC POST SYSTEMS |
| Classification | Sterilizer, Boiling Water |
| Applicant | PREAT CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ECG |
| CFR Regulation Number | 872.6710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-04-10 |
| Decision Date | 1981-05-13 |