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

AcuSnare Polypectomy Snare - Duckbill

K Number: K191048 · Decision Jul 18, 2019
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
62
Applicant Total
125
Review Days
90

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Basic Information

Device Name
AcuSnare Polypectomy Snare - Duckbill
K Number
K191048
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wilson-Cook Medical, Inc.
Date Received
April 19, 2019
Decision Date
July 18, 2019
Product Code
FDI
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
FDI Snare, Flexible

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