K864976 is an FDA 510(k) clearance for the SOLUSET CALCIUM DEMINERALIZING SOLUTION. This device is classified as a File, Pulp Canal, Endodontic (Class I - General Controls, product code EKS).
Submitted by Endo Technic Corp. (Natick, US). The FDA issued a Cleared decision on February 27, 1987, 70 days after receiving the submission on December 19, 1986.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.4565.
| 510(k) Number | K864976 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 19, 1986 |
| Decision Date | February 27, 1987 |
| Days to Decision | 70 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | EKS — File, Pulp Canal, Endodontic |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 872.4565 |