FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

URESIL PERCUTANEOUS DRAINAGE CATHETERS WITH HYDROPHILIC COATING

K Number: K981344 · Decision Sep 10, 1998
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
55
Applicant Total
45
Review Days
154

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Basic Information

Device Name
URESIL PERCUTANEOUS DRAINAGE CATHETERS WITH HYDROPHILIC COATING
K Number
K981344
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Uresil Corp.
Date Received
April 9, 1998
Decision Date
September 10, 1998
Product Code
LJE
Advisory Committee
Unknown
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LJE Catheter, Nephrostomy

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Other Clearances by Uresil Corp.

K Number Device Name
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K980278 URESIL VASCU-FLO INFUSION CATHETER
K980282 URESIL DILATOR WITH RADIOPAQUE MARKER
K980889 URESIL NEPHRO-URETERAL STENT
K972582 URESIL GUIDEWIRE
K972583 URESIL GENERAL PURPOSE DRAINAGE CATHETER, URESIL NEPHROSTOMY CATHETER, URESIL BILIARY CATHETER, URESIL NEPHRO-URETERAL S
K953923 URESIL INTRODUCING NEEDLE
K945934 URESIL(R) GUIDEWIRE
K942688 NEPHRO-URETERAL STENT
K944784 MINI-OP LAPAROSCOPIC LASSO
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