Estill Medical Technologies, Inc

FDA Regulatory Profile

Estill Medical Technologies, Inc appears in FDA public data with 1 recall, 2 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0101-2015, Class II) was initiated on July 25, 2014. Its most recent 510(k) clearance was granted on July 26, 2001.

Summary

Total Recalls
1
510(k) Clearances
2
Inspections
2
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0101-2015Class IIUltra Battery 1 Model: TA-UB1 NSN: 6515-01-592-5803 The Ultra Battery 1 (TA-UB1) is a rechargeabJuly 25, 2014

Recent 510(k) Clearances

K-NumberDeviceDate
K012031MODIFICATION TO THERMAL ANGELJuly 26, 2001
K984640THERMAL ANGELJuly 1, 1999