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AcuPulse (previously called AcuPulse 30/40 ST) +2 more models
FDA 510(k)Class II (US FDA 510(k))
510(k) K180597
by Lumenis Inc.
Identifiers
- 510(k) Number
- K180597 FDA 510(k)
- FDA Product Code
- GEX FDA 510(k)
- Models / Variants
- AcuPulse 40W G FDA 510(k)AcuPulse DUO FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.4810 FDA 510(k)
- Regulation Number
- 878.4810 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
AcuPulse (previously called AcuPulse 30/40 ST) +2 more models by Lumenis Inc. — Class II — FDA_510K — listed in FDA 510(k) — 3 models
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K180597 | Class II | Active |
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Manufacturer
- Manufacturer
- Lumenis Inc.
- FDA Applicant
- Lumenis, Ltd.
Sources (1)
- FDA 510(k) K180597 24 fields · synced Jun 18, 2026