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

PlumeSafe X5 Smoke Management System

K Number: K240127 · Decision Aug 5, 2024
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
74
Applicant Total
82
Review Days
201

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Basic Information

Device Name
PlumeSafe X5 Smoke Management System
K Number
K240127
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5070
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Conmed Corporation
Date Received
January 17, 2024
Decision Date
August 5, 2024
Product Code
FYD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FYD Apparatus, Exhaust, Surgical

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