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

ELITECORE FULL CORE BIOPSY DEVICE 18GAX10CM, 18GAX15CM, 18GAX20, WITH/HILITIER 18GAX10CM , W/HILITER 18GAX15CM

K Number: K112945 · Decision Nov 3, 2011
Classifications
1
FEI Numbers
207
Registration Numbers
207
Same Product Code
360
Applicant Total
4
Review Days
30

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Basic Information

Device Name
ELITECORE FULL CORE BIOPSY DEVICE 18GAX10CM, 18GAX15CM, 18GAX20, WITH/HILITIER 18GAX10CM , W/HILITER 18GAX15CM
K Number
K112945
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Inrad, Inc.
Date Received
October 4, 2011
Decision Date
November 3, 2011
Product Code
KNW
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
KNW Instrument, Biopsy

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