FIBERLITE, FIBERLITE HS AND FIBERSEAL — Jeneric/Pentron, Inc. (510(k) K884038)
FIBERLITE, FIBERLITE HS AND FIBERSEAL — Jeneric/Pentron, Inc. (510(k) K884038) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: FIBERLITE, FIBERLITE HS AND FIBERSEAL; Applicant: Jeneric/Pentron, Inc.; Clearance track: 510(k).
| Device name | FIBERLITE, FIBERLITE HS AND FIBERSEAL |
|---|---|
| Applicant | Jeneric/Pentron, Inc. |
| Clearance track | 510(k) |
| Submission number | K884038 |
| Decision | Substantially Equivalent |
| Decision date | 1988-12-07 |
| Date received | 1988-09-26 |
| Product code | EBF |
| Device class | 2 |
| Medical specialty | Dental |
| Applicant location | CT, US |
| Source | openFDA device |
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