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

FDA 510(k) Number Submission Date Device Name Applicant
K162611 09/19/2016 PeriFLEX SPIRATION, INC.
K170990 04/03/2017 Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator Spiration, Inc.
K171492 05/22/2017 B7 2C Occlusion Balloon Spiration, Inc.
K152922 10/02/2015 ViziShot FLEX SPIRATION, INC.
K142909 10/06/2014 Flexible 19G EBUS Needle SPIRATION, INC.


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