FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

APLAN A.V. FISTULA NEEDLE SET

K Number: K112734 · Decision Apr 24, 2012
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
78
Applicant Total
1
Review Days
217

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Basic Information

Device Name
APLAN A.V. FISTULA NEEDLE SET
K Number
K112734
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aplan Well Enterprise Co., Ltd.
Date Received
September 20, 2011
Decision Date
April 24, 2012
Product Code
FIE
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
FIE Needle, Fistula

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