CANDELA FAMILY OF PULSED DYE LASER SYSTEMS, MODELS VBEAM, CBEAM, SPTL-1B — Candela Corp. (510(k) K043251)
CANDELA FAMILY OF PULSED DYE LASER SYSTEMS, MODELS VBEAM, CBEAM, SPTL-1B — Candela Corp. (510(k) K043251) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: CANDELA FAMILY OF PULSED DYE LASER SYSTEMS, MODELS VBEAM, CBEAM, SPTL-1B; Applicant: Candela Corp.; Clearance track: 510(k).
| Device name | CANDELA FAMILY OF PULSED DYE LASER SYSTEMS, MODELS VBEAM, CBEAM, SPTL-1B |
|---|---|
| Applicant | Candela Corp. |
| Clearance track | 510(k) |
| Submission number | K043251 |
| Decision | Substantially Equivalent |
| Decision date | 2005-02-09 |
| Date received | 2004-11-23 |
| Product code | GEX |
| Device class | 2 |
| Medical specialty | General, Plastic Surgery |
| Applicant location | MA, US |
| Source | openFDA device |
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