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

Clear-Jet Injection Catheter

K Number: K181690 · Decision Dec 21, 2018
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
88
Applicant Total
11
Review Days
178

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Basic Information

Device Name
Clear-Jet Injection Catheter
K Number
K181690
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Finemedix Co., Ltd.
Date Received
June 26, 2018
Decision Date
December 21, 2018
Product Code
FBK
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
FBK Endoscopic Injection Needle, Gastroenterology-Urology

Similar 510(k) Clearances

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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
K242134 ClearCap Distal Attachment
K231267 ClearTip
K202616 ClearCap Distal Attachment
K200217 ClearEndoclip
K183021 ClearEndoclip
K183289 ClearGrasp Snare
K180363 Clear-Tip EUS-FNA
Search all 11 clearances from Finemedix Co., Ltd. →