FLUORILAQ SODIUM FLUORIDE CAVITY VARNISH — Pascal Co., Inc. (510(k) K090597)
FLUORILAQ SODIUM FLUORIDE CAVITY VARNISH — Pascal Co., Inc. (510(k) K090597) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: FLUORILAQ SODIUM FLUORIDE CAVITY VARNISH; Applicant: Pascal Co., Inc.; Clearance track: 510(k).
| Device name | FLUORILAQ SODIUM FLUORIDE CAVITY VARNISH |
|---|---|
| Applicant | Pascal Co., Inc. |
| Clearance track | 510(k) |
| Submission number | K090597 |
| Decision | Substantially Equivalent |
| Decision date | 2009-03-16 |
| Date received | 2009-03-05 |
| Product code | LBH |
| Device class | 2 |
| Medical specialty | Dental |
| Applicant location | WA, US |
| Source | openFDA device |
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