K953604 is an FDA 510(k) clearance for the SHAPING HEDSTROM N.T.. This device is classified as a File, Pulp Canal, Endodontic (Class I - General Controls, product code EKS).
Submitted by Sybron Dental Specialties, Inc. (Glendora, US). The FDA issued a Cleared decision on September 28, 1995, 57 days after receiving the submission on August 2, 1995.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.4565.
| 510(k) Number | K953604 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 02, 1995 |
| Decision Date | September 28, 1995 |
| Days to Decision | 57 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EKS — File, Pulp Canal, Endodontic |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 872.4565 |