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

Agnes

K Number: K192728 · Decision Oct 24, 2019
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
7
Review Days
27

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Basic Information

Device Name
Agnes
K Number
K192728
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Agnes Medical Co., Ltd.
Date Received
September 27, 2019
Decision Date
October 24, 2019
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

Similar 510(k) Clearances

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Other Clearances by Agnes Medical Co., Ltd.

K Number Device Name
K250217 AGNES Ultra
K243713 Single Use RF Surgical Electrode (Needle Type) (AN-B, AN-C, AN-E, AN-I, AN-S, AN-W3A, AN-F3A, AN-IL, AN-SL, AN-W3B, AN-F1A, AN-F3B, AN-B3A)
K242469 RFMagik Lite
K230837 PlazMagik
K223805 Agnes
K203013 AGNES