FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Soniquence Reusable Neutral Plate

K Number: K220071 · Decision Feb 3, 2022
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
6
Review Days
24

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Basic Information

Device Name
Soniquence Reusable Neutral Plate
K Number
K220071
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
Soniquence, LLC
Date Received
January 10, 2022
Decision Date
February 3, 2022
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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