SPETEMP EF — Ultradent Products, Inc. (510(k) K964809)
SPETEMP EF — Ultradent Products, Inc. (510(k) K964809) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: SPETEMP EF; Applicant: Ultradent Products, Inc.; Clearance track: 510(k).
| Device name | SPETEMP EF |
|---|---|
| Applicant | Ultradent Products, Inc. |
| Clearance track | 510(k) |
| Submission number | K964809 |
| Decision | Substantially Equivalent |
| Decision date | 1997-01-02 |
| Date received | 1996-11-29 |
| Product code | EMA |
| Device class | 2 |
| Medical specialty | Dental |
| Applicant location | UT, US |
| Source | openFDA device |
🔍 Search all device clearances →
$1999/mo
Try DeviceClear →