REPRO-MED SYSTEMS INFUSION DEVICE — Repro-Med Systems, Inc. (510(k) K844401)
REPRO-MED SYSTEMS INFUSION DEVICE — Repro-Med Systems, Inc. (510(k) K844401) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: REPRO-MED SYSTEMS INFUSION DEVICE; Applicant: Repro-Med Systems, Inc.; Clearance track: 510(k).
| Device name | REPRO-MED SYSTEMS INFUSION DEVICE |
|---|---|
| Applicant | Repro-Med Systems, Inc. |
| Clearance track | 510(k) |
| Submission number | K844401 |
| Decision | Substantially Equivalent |
| Decision date | 1985-03-12 |
| Date received | 1984-11-13 |
| Product code | FRN |
| Device class | 2 |
| Medical specialty | General Hospital |
| Applicant location | NY, US |
| Source | openFDA device |
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