FDA 510(k) Applications Submitted by NEUWAVE MEDICAL, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K232227 |
07/27/2023 |
ABLATE-IQ |
NeuWave Medical, Inc. |
| K200081 |
01/15/2020 |
NEUWAVE Microwave Ablation System and Accessories |
NeuWave Medical, Inc. |
| K130399 |
02/19/2013 |
CERTUS 140 CERTUSURGGT SURGICAL TOOL |
NEUWAVE MEDICAL, INC. |
| K171022 |
04/05/2017 |
Ablation Confirmation |
NeuWave Medical, Inc. |
| K161285 |
05/09/2016 |
Ablation Confirmation |
NEUWAVE MEDICAL, INC. |
| K113237 |
11/02/2011 |
CERTUS 140 2.45GHZ ABLATION SYSTEM |
NEUWAVE MEDICAL, INC. |
| K163118 |
11/08/2016 |
FLEX Microwave Ablation System and Accessories |
NEUWAVE MEDICAL, INC. |
| K173756 |
12/11/2017 |
Certus 140 2.45GHz Ablation System |
NeuWave Medical, Inc. |
| K231738 |
06/14/2023 |
NEUWAVEÖ Microwave Ablation System and Accessories |
NeuWave Medical, Inc. |
| K192427 |
09/05/2019 |
Ablation Confirmation |
NeuWave Medical, Inc. |
|
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