KIPPMED I.V. MANIFOLD — The Kipp Group (510(k) K000152)
KIPPMED I.V. MANIFOLD — The Kipp Group (510(k) K000152) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: KIPPMED I.V. MANIFOLD; Applicant: The Kipp Group; Clearance track: 510(k).
| Device name | KIPPMED I.V. MANIFOLD |
|---|---|
| Applicant | The Kipp Group |
| Clearance track | 510(k) |
| Submission number | K000152 |
| Decision | Substantially Equivalent |
| Decision date | 2000-02-29 |
| Date received | 2000-01-19 |
| Product code | FPA |
| Device class | 2 |
| Medical specialty | General Hospital |
| Applicant location | CA, US |
| Source | openFDA device |
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