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

AveCure Microwave Coagulation-Ablation Generator, AveCure Microwave Large Antenna-Probe, AveCure Microwave Medium Antenna-Probe, AveCure Microwave Small Antenna-Probe, AveCure Microwave Mini Antenna-Probe

K Number: K143203 · Decision Aug 26, 2015
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
67
Applicant Total
3
Review Days
292

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Basic Information

Device Name
AveCure Microwave Coagulation-Ablation Generator, AveCure Microwave Large Antenna-Probe, AveCure Microwave Medium Antenna-Probe, AveCure Microwave Small Antenna-Probe, AveCure Microwave Mini Antenna-Probe
K Number
K143203
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
Medwaves Incorporated
Date Received
November 7, 2014
Decision Date
August 26, 2015
Product Code
NEY
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
NEY System, Ablation, Microwave And Accessories

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NEY), ordered by most recent decision date.

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Other Clearances by Medwaves Incorporated

K Number Device Name
K083537 MODIFICATION TO MEDWAVES MICROWAVE COAGULATION/ABLATION SYSTEM
K070356 MEDWAVES MICROWAVE COAGULATION/ABLATION SYSTEM