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

Density

K Number: K230663 · Decision Aug 14, 2023
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
15
Review Days
157

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Basic Information

Device Name
Density
K Number
K230663
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jeisys Medical, Inc.
Date Received
March 10, 2023
Decision Date
August 14, 2023
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

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