PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOG — Minnesota Laser Corp. (510(k) K854472)
PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOG — Minnesota Laser Corp. (510(k) K854472) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOG; Applicant: Minnesota Laser Corp.; Clearance track: 510(k).
| Device name | PORTALASE 300 CARBON DIOXIDE SURG LASER DERMATOLOG |
|---|---|
| Applicant | Minnesota Laser Corp. |
| Clearance track | 510(k) |
| Submission number | K854472 |
| Decision | Substantially Equivalent |
| Decision date | 1986-02-11 |
| Date received | 1985-11-06 |
| Product code | GEX |
| Device class | 2 |
| Medical specialty | General, Plastic Surgery |
| Applicant location | MN, US |
| Source | openFDA device |
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$1999/mo
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