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

ClearGrasp Snare

K Number: K183289 · Decision Mar 6, 2019
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
62
Applicant Total
11
Review Days
100

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ClearGrasp Snare
K Number
K183289
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
November 26, 2018
Decision Date
March 6, 2019
Product Code
FDI
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
FDI Snare, Flexible

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FDI), ordered by most recent decision date.

View all

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
K181690 Clear-Jet Injection Catheter
K180363 Clear-Tip EUS-FNA
Search all 11 clearances from Finemedix Co., Ltd. →