FDA 510(k) Applications Submitted by NORA HADDING

FDA 510(k) Number	Submission Date	Device Name	Applicant
K161384	05/19/2016	Lithoplasty Peripheral Balloon Dilatation Catheter, Lithoplasty Generator and Connector Cable, Lithoplasty Connector Cable	Shockwave Medical, Inc.
K961679	05/01/1996	TRANSVENOUS, PERMANENT TINED TARGET TIP PACING LEADS/TRANSVENOUS, PERMANENT SCREW-IN PACING LEADS	MEDTRONIC VASCULAR
K961936	05/20/1996	MODEL 2188 CORONARY SINUS LEAD.	MEDTRONIC VASCULAR
K972242	06/16/1997	REVEAL INSERTABLE LOOP RECORDER (ILR) SYSTEM	MEDTRONIC VASCULAR
K994331	12/23/1999	REVEAL PLUS INSERTABLE LOOP RECORDER SYSTEM, MODEL 9526 IMPLANTED RECORDER AND MODEL 6191 PATIENT ACTIVATOR	MEDTRONIC VASCULAR