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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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