ACMI BIPOLAR HEMOSTATIC SOURCE — American Cystocope Makers, Inc. (510(k) K812637)
ACMI BIPOLAR HEMOSTATIC SOURCE — American Cystocope Makers, Inc. (510(k) K812637) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: ACMI BIPOLAR HEMOSTATIC SOURCE; Applicant: American Cystocope Makers, Inc.; Clearance track: 510(k).
| Device name | ACMI BIPOLAR HEMOSTATIC SOURCE |
|---|---|
| Applicant | American Cystocope Makers, Inc. |
| Clearance track | 510(k) |
| Submission number | K812637 |
| Decision | Substantially Equivalent |
| Decision date | 1981-10-26 |
| Date received | 1981-09-15 |
| Product code | GEI |
| Device class | 2 |
| Medical specialty | General, Plastic Surgery |
| Applicant location | IL, US |
| Source | openFDA device |
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