AUROFLUID 22 — Metalor Dental USA Corp. (510(k) K970044)
AUROFLUID 22 — Metalor Dental USA Corp. (510(k) K970044) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: AUROFLUID 22; Applicant: Metalor Dental USA Corp.; Clearance track: 510(k).
| Device name | AUROFLUID 22 |
|---|---|
| Applicant | Metalor Dental USA Corp. |
| Clearance track | 510(k) |
| Submission number | K970044 |
| Decision | Substantially Equivalent |
| Decision date | 1997-03-05 |
| Date received | 1997-01-06 |
| Product code | EJS |
| Device class | 2 |
| Medical specialty | Dental |
| Applicant location | MA, US |
| Source | openFDA device |
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$1999/mo
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