The following data is part of a premarket notification filed by Charles Scharf with the FDA for Dds-zr.
| Device ID | K041645 |
| 510k Number | K041645 |
| Device Name: | DDS-ZR |
| Classification | Powder, Porcelain |
| Applicant | CHARLES SCHARF 7375 S. PEORIA ST. #105 B-10 Englewood, CO 80112 |
| Contact | Chris Scharf |
| Correspondent | Chris Scharf CHARLES SCHARF 7375 S. PEORIA ST. #105 B-10 Englewood, CO 80112 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-06-17 |
| Decision Date | 2004-07-09 |
| Summary: | summary |