Zdrowie i gospodarka · 14/08/2008

FDA Corrects Final Rule on Bone Sonometer Devices Reclassification

The FDA is revising a 2008 rule reclassifying bone sonometer devices from class III to class II, subject to special controls, to correct an error affecting small businesses. The FDA corrected the error in a final rule published in the Federal Register on July 17, 2008 (73 FR 40967).