SINGLE USE NEEDLE ELECTRODE — Aspen Laboratories, Inc. (510(k) K780975)
SINGLE USE NEEDLE ELECTRODE — Aspen Laboratories, Inc. (510(k) K780975) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: SINGLE USE NEEDLE ELECTRODE; Applicant: Aspen Laboratories, Inc.; Clearance track: 510(k).
| Device name | SINGLE USE NEEDLE ELECTRODE |
|---|---|
| Applicant | Aspen Laboratories, Inc. |
| Clearance track | 510(k) |
| Submission number | K780975 |
| Decision | Substantially Equivalent |
| Decision date | 1978-06-22 |
| Date received | 1978-06-09 |
| Product code | GEI |
| Device class | 2 |
| Medical specialty | General, Plastic Surgery |
| Applicant location | IL, US |
| Source | openFDA device |
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$1999/mo
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