FDA 510(k) Applications for Medical Device Product Code: PIE ()

FDA 510(k) Applications for Medical Device Product Code "PIE"

FDA 510(k) Number	Applicant	Device Name	Decision Date
K172128	Crospon Ltd.	EsoFLIP« ES-310 Balloon Catheter	11/22/2017
K142000	CROSPON, LTD.	ESOFLIP ES	09/25/2014

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