Arteria Medical Science, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K021210ARTERIA OCCLUSION BALLOONOctober 28, 2002
K021293ARTERIA BLOOD FILTERAugust 22, 2002
K001917PARODI CATHETER FOR ANGIOGRAPHY (PARCA)June 6, 2001