PENOX DUAL FEED MANIFOLD — Penox Technologies, Inc. (510(k) K851216)
PENOX DUAL FEED MANIFOLD — Penox Technologies, Inc. (510(k) K851216) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: PENOX DUAL FEED MANIFOLD; Applicant: Penox Technologies, Inc.; Clearance track: 510(k).
| Device name | PENOX DUAL FEED MANIFOLD |
|---|---|
| Applicant | Penox Technologies, Inc. |
| Clearance track | 510(k) |
| Submission number | K851216 |
| Decision | Substantially Equivalent |
| Decision date | 1985-06-18 |
| Date received | 1985-03-26 |
| Product code | CAM |
| Device class | 1 |
| Medical specialty | Anesthesiology |
| Applicant location | PA, US |
| Source | openFDA device |
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