Zdrowie i gospodarka · 09/03/2001
FDA Reclassifies Home Uterine Activity Monitor for Women with Preterm Delivery History
The FDA has reclassified the Corometrics Model 770 Home Uterine Activity Monitoring System from Class III to Class II, special controls, for use in women with a previous preterm delivery to aid in preterm labor detection, and made it codified in the Code of Federal Regulations.