Aframe Digital, Inc.

FDA Regulatory Profile

Aframe Digital, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 19, 2012.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K122333MOBILECARE MONITORNovember 19, 2012
K090138MOBILECARE MONITOR, MODEL 2100April 24, 2009