FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

WILSON-COOK ULTRASOUND BIOPSY NEEDLE

K Number: K013356 · Decision Oct 19, 2001
Classifications
1
FEI Numbers
128
Registration Numbers
128
Same Product Code
132
Applicant Total
125
Review Days
9

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Basic Information

Device Name
WILSON-COOK ULTRASOUND BIOPSY NEEDLE
K Number
K013356
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wilson-Cook Medical, Inc.
Date Received
October 10, 2001
Decision Date
October 19, 2001
Product Code
FCG
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
FCG Biopsy Needle

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