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

URINARY DIVERSION STENT

K Number: K830803 · Decision May 5, 1983
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
55
Applicant Total
52
Review Days
52

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Basic Information

Device Name
URINARY DIVERSION STENT
K Number
K830803
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Van-Tec, Inc.
Date Received
March 14, 1983
Decision Date
May 5, 1983
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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K880095 BERGER PROSTATE CULTURE CYTOLOGY BRUSH
K880099 VAN-TEC BLADDER EVACUATOR
K880094 VAN-TEC ENDOPYELOTOMY KNIFE
K874112 VAN-TEC DOUBLE OCCLUSION BALLOON CATHETER
K871777 VAN-TEC REUSABLE HELICAL STONE BASKET
K871779 HELICAL STONE BASKET (DISPOSABLE)
K870679 VAN-TEC MODULAR FLEXIBLE CYSTOURETHROSCOPE
K870557 VAN-TEC PUMPING SYSTEM
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