K003373 is an FDA 510(k) clearance for the PROCAD ADD-ON. This device is classified as a Powder, Porcelain (Class II - Special Controls, product code EIH).
Submitted by Ivoclar North America, Inc. (Amherst, US). The FDA issued a Cleared decision on November 28, 2000, 29 days after receiving the submission on October 30, 2000.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.6660.
| 510(k) Number | K003373 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 30, 2000 |
| Decision Date | November 28, 2000 |
| Days to Decision | 29 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
| Product Code | EIH — Powder, Porcelain |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.6660 |