Celleration, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K140782ULTRAMIST SYSTEM, ULTRAMIST GENERATOR, ULTRAMIST TREATMENT WAND, ULTRAMIST APPLICATORAugust 13, 2014
K122246MIST 360 SINGLE USE APPLICATOR KIT, MIST 360 SINGLE USE APPLICATOR KIT, CASE OF 12August 13, 2012
K050129CELLERATION MIST THERAPY SYSTEM 5.1May 17, 2005
DEN040004CELLERATION MIST THERAPY SYSTEMJune 25, 2004