FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

ClearTip FNA and FNB Types

K Number: K250994 · Decision Aug 21, 2025
Classifications
1
FEI Numbers
128
Registration Numbers
128
Same Product Code
132
Applicant Total
11
Review Days
142

Basic Information

Device Name
ClearTip FNA and FNB Types
K Number
K250994
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Finemedix Co., Ltd.
Date Received
April 1, 2025
Decision Date
August 21, 2025
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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Other Clearances by Finemedix Co., Ltd.

K Number Device Name
K251478 ClearTip TBNA Type
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K242134 ClearCap Distal Attachment
K231267 ClearTip
K202616 ClearCap Distal Attachment
K200217 ClearEndoclip
K183021 ClearEndoclip
K183289 ClearGrasp Snare
K181690 Clear-Jet Injection Catheter
K180363 Clear-Tip EUS-FNA
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