Aristo Medical Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K961060ARISTO ESOPHAGEAL STETHOSCOPEJune 19, 1996
K960251COMSAT ADULT,PEDIATRIC,INFANT,NEONATAL DISPOSABLE SENSOR AND COMSAT REUSABLE FINGER SENSORMarch 26, 1996
K953817ARISTO MEDICAL MODEL 2101 PATIENT MONITORNovember 22, 1995
K920966SDI OXYGEN/DIGITAL OXYGEN TRANSDUCERS (DOT)July 16, 1993