FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AL ASKARI PERCUTANEOUS ACCESS NEEDLE HOLDER

K Number: K851162 · Decision Apr 15, 1985
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
43
Applicant Total
52
Review Days
24

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Basic Information

Device Name
AL ASKARI PERCUTANEOUS ACCESS NEEDLE HOLDER
K Number
K851162
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.4730
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Van-Tec, Inc.
Date Received
March 22, 1985
Decision Date
April 15, 1985
Product Code
KOA
Advisory Committee
Gastroenterology, Urology
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
KOA Surgical Instruments, G-U, Manual (And Accessories)

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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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