WEINGART MODEL 1000 SUNLAMP PRODUCT — Weingart, Inc. (510(k) K863518)
WEINGART MODEL 1000 SUNLAMP PRODUCT — Weingart, Inc. (510(k) K863518) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: WEINGART MODEL 1000 SUNLAMP PRODUCT; Applicant: Weingart, Inc.; Clearance track: 510(k).
| Device name | WEINGART MODEL 1000 SUNLAMP PRODUCT |
|---|---|
| Applicant | Weingart, Inc. |
| Clearance track | 510(k) |
| Submission number | K863518 |
| Decision | Substantially Equivalent |
| Decision date | 1986-10-02 |
| Date received | 1986-09-09 |
| Product code | FTC |
| Device class | 2 |
| Medical specialty | General, Plastic Surgery |
| Applicant location | IN, US |
| Source | openFDA device |
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$1999/mo
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