Home / Companies / Maxi-Aids, Inc.

Maxi-Aids, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K041778REIZEN TALKING BLOOD PRESSURE MONITOR, MODEL #SF860TAugust 31, 2004
K960567HF MEGA EAROctober 16, 1996