PULPDENT CAVITY PREPARATION II, PULPDENT CAVITY PREPARATION II WUTH FLUORIDE — Pulpdent Corp. (510(k) K994181)
PULPDENT CAVITY PREPARATION II, PULPDENT CAVITY PREPARATION II WUTH FLUORIDE — Pulpdent Corp. (510(k) K994181) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: PULPDENT CAVITY PREPARATION II, PULPDENT CAVITY PREPARATION II WUTH FLUORIDE; Applicant: Pulpdent Corp.; Clearance track
| Device name | PULPDENT CAVITY PREPARATION II, PULPDENT CAVITY PREPARATION II WUTH FLUORIDE |
|---|---|
| Applicant | Pulpdent Corp. |
| Clearance track | 510(k) |
| Submission number | K994181 |
| Decision | Substantially Equivalent |
| Decision date | 2000-02-29 |
| Date received | 1999-12-10 |
| Product code | LBH |
| Device class | 2 |
| Medical specialty | Dental |
| Applicant location | MA, US |
| Source | openFDA device |
🔍 Search all device clearances →
$1999/mo
Try DeviceClear →