Zdrowie i gospodarka · 11/02/2000
FDA Reclassifies Nd:YAG Laser for Peripheral Iridotomy from Class III to Class II
The FDA has issued a letter to Escalon Medical Corporation, reclassifying the Neodymium:Yttrium:Aluminum:Garnet (Nd:YAG) Laser for use in peripheral iridotomy from a Class III device to a Class II device with special controls, as per the Code of Federal Regulations (CFR).
Source: Federal Register — Food and Drug AdministrationOpen original release →