The following data is part of a premarket notification filed by Dr. Joseph E. Grasso, D.d.s. with the FDA for Coupling Device For Dental Prosthesis.
| Device ID | K950259 |
| 510k Number | K950259 |
| Device Name: | COUPLING DEVICE FOR DENTAL PROSTHESIS |
| Classification | Attachment, Precision, All |
| Applicant | DR. JOSEPH E. GRASSO, D.D.S. 4 ROSWELL RD. West Simsbury, CT 06092 |
| Contact | Joseph E Grasso |
| Correspondent | Joseph E Grasso DR. JOSEPH E. GRASSO, D.D.S. 4 ROSWELL RD. West Simsbury, CT 06092 |
| Product Code | EGG |
| CFR Regulation Number | 872.3165 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-01-23 |
| Decision Date | 1996-12-06 |