FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Multi-Band Ligator

K Number: K213223 · Decision Jun 6, 2022
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
21
Applicant Total
6
Review Days
250

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Basic Information

Device Name
Multi-Band Ligator
K Number
K213223
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4400
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beijing Zksk Technology Co., Ltd.
Date Received
September 29, 2021
Decision Date
June 6, 2022
Product Code
FHN
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
FHN Ligator, Hemorrhoidal

Similar 510(k) Clearances

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Other Clearances by Beijing Zksk Technology Co., Ltd.

K Number Device Name
K242192 Disposable Sphincterotome
K231721 Disposable Hot Biopsy Forceps
K213217 Disposable hemoclip
K213222 Disposable Polypectomy Snare
K213239 Endoscopic Injection Needle