Zdrowie i gospodarka · 30.09.1998
Medical Devices; Exemptions From Premarket Notification; Class II Devices
The Food and Drug Administration (FDA) is publishing a list of petitions requesting exemption from the premarket notification requirements for certain class II devices. FDA is publishing this notice in order to obtain comments on these petitions in accordance with procedures established by the Food and Drug Administration Modernization Act of 1997 (FDAMA).