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

ClearCap Distal Attachment

K Number: K242134 · Decision Aug 20, 2024
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
92
Applicant Total
11
Review Days
29

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Basic Information

Device Name
ClearCap Distal Attachment
K Number
K242134
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Finemedix Co., Ltd.
Date Received
July 22, 2024
Decision Date
August 20, 2024
Product Code
OCX
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
OCX Endoscopic Irrigation/Suction System

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Other Clearances by Finemedix Co., Ltd.

K Number Device Name
K251478 ClearTip TBNA Type
K250994 ClearTip FNA and FNB Types
K242857 ClearHemograsper
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. →