K240543
- 510(k) number
- K240543
- Device name
- Rapido Medical Laser (Rapido MED, Rapido Derma, Rapido ENT, Rapido Podia)
- Applicant
- Medency S.R.L. IT
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2024-10-24
- Date received
- 2024-02-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K240543
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.