FDA 510(k) Applications Submitted by KATHY SIMPSON
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K180237 |
01/29/2018 |
Rezum System |
NxThera, 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. |
K162721 |
09/29/2016 |
Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator |
ALLIQUA BIOMEDICAL, INC. |
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