FDA 510(k) Applications Submitted by CELLERATION, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K050129 01/19/2005 CELLERATION MIST THERAPY SYSTEM 5.1 CELLERATION, INC.
K140782 03/31/2014 ULTRAMIST SYSTEM, ULTRAMIST GENERATOR, ULTRAMIST TREATMENT WAND, ULTRAMIST APPLICATOR CELLERATION, INC.
K122246 07/27/2012 MIST 360 SINGLE USE APPLICATOR KIT, MIST 360 SINGLE USE APPLICATOR KIT, CASE OF 12 CELLERATION, INC.


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