The following data is part of a premarket notification filed by Austenal Dental, Inc. with the FDA for Base, Denture, Relining, Repairing, Rebasing,resin.
| Device ID | K883799 |
| 510k Number | K883799 |
| Device Name: | BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN |
| Classification | Resin, Denture, Relining, Repairing, Rebasing |
| Applicant | AUSTENAL DENTAL, INC. 5101 S. KEELER AVE. Chicago, IL 60632 |
| Contact | Ronald Dudek |
| Correspondent | Ronald Dudek AUSTENAL DENTAL, INC. 5101 S. KEELER AVE. Chicago, IL 60632 |
| Product Code | EBI |
| CFR Regulation Number | 872.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-07 |
| Decision Date | 1988-10-20 |