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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
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