FDA 510(k) Applications Submitted by LEV MELINYSHYN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K980282	01/26/1998	URESIL DILATOR WITH RADIOPAQUE MARKER	URESIL CORP.
K980889	03/09/1998	URESIL NEPHRO-URETERAL STENT	URESIL CORP.
K981344	04/09/1998	URESIL PERCUTANEOUS DRAINAGE CATHETERS WITH HYDROPHILIC COATING	URESIL CORP.
K972582	07/10/1997	URESIL GUIDEWIRE	URESIL CORP.
K972583	07/10/1997	URESIL GENERAL PURPOSE DRAINAGE CATHETER, URESIL NEPHROSTOMY CATHETER, URESIL BILIARY CATHETER, URESIL NEPHRO-URETERAL S	URESIL CORP.
K093653	11/25/2009	URESIL GASTROSTOMY CATHETER KIT , MODEL GCL-630HBK	URESIL, LLC