FDA 510(k), K180211, Freezpoint

FDA 510(k), K180211, Freezpoint

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510(K) Number: K180211
Device Name: Freezpoint
Manufacturer: Sam Niedbala
Device Classification Name: Unit, Cryosurgical, Accessories
Regulation Number: GEH
Classification Product Code: 01/25/2018
Date Received: 03/21/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

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