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

ClearHemograsper

K Number: K242857 · Decision May 21, 2025
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
45
Applicant Total
11
Review Days
243

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Basic Information

Device Name
ClearHemograsper
K Number
K242857
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Finemedix Co., Ltd.
Date Received
September 20, 2024
Decision Date
May 21, 2025
Product Code
KGE
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
KGE Forceps, Biopsy, Electric

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Other Clearances by Finemedix Co., Ltd.

K Number Device Name
K251478 ClearTip TBNA Type
K250994 ClearTip FNA and FNB Types
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
Search all 11 clearances from Finemedix Co., Ltd. →