DRI-CLAVE LIQUID KLEENZALL — Columbus Dental Mfg. Co. (510(k) K880754)
DRI-CLAVE LIQUID KLEENZALL — Columbus Dental Mfg. Co. (510(k) K880754) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: DRI-CLAVE LIQUID KLEENZALL; Applicant: Columbus Dental Mfg. Co.; Clearance track: 510(k).
| Device name | DRI-CLAVE LIQUID KLEENZALL |
|---|---|
| Applicant | Columbus Dental Mfg. Co. |
| Clearance track | 510(k) |
| Submission number | K880754 |
| Decision | Substantially Equivalent |
| Decision date | 1988-05-12 |
| Date received | 1988-02-25 |
| Product code | EHZ |
| Device class | 1 |
| Medical specialty | Dental |
| Applicant location | MO, US |
| Source | openFDA device |
🔍 Search all device clearances →
$1999/mo
Try DeviceClear →