K-number	K240543
Device name	Rapido Medical Laser (Rapido MED, Rapido Derma, Rapido ENT, Rapido Podia)
Applicant	Medency S.R.L.
Product code	GEX
Device class	Class II
Decision date	Oct 24, 2024
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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Rapido Medical Laser (Rapido MED, Rapido Derma, Rapido ENT, Rapido Podia)

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