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

Ablation Confirmation

K Number: K150313 · Decision Jul 9, 2015
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
15
Review Days
150

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Basic Information

Device Name
Ablation Confirmation
K Number
K150313
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neuwave Medical, Inc.
Date Received
February 9, 2015
Decision Date
July 9, 2015
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LLZ System, Image Processing, Radiological

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Other Clearances by Neuwave Medical, Inc.

K Number Device Name
K232227 ABLATE-IQ
K231738 NEUWAVE™ Microwave Ablation System and Accessories
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K200081 NEUWAVE Microwave Ablation System and Accessories
K192427 Ablation Confirmation
K173756 Certus 140 2.45GHz Ablation System
K171022 Ablation Confirmation
K163118 FLEX Microwave Ablation System and Accessories
K161285 Ablation Confirmation
K160936 Certus 140 2.45GHz Ablation System
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