Neuwave Medical, Inc.
Neuwave Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2024.
Top product codes for Neuwave Medical, Inc.
Recent clearances by Neuwave Medical, Inc.
- K232227 — ABLATE-IQ
- K231738 — NEUWAVE Microwave Ablation System and Accessories
- K220472 — NEUWAVE Microwave Ablation System and Accessories
- 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
- K150313 — Ablation Confirmation
- K130399 — CERTUS 140 CERTUSURGGT SURGICAL TOOL
- K122217 — CERTUS 140 2.45GHZ ABLATION SYSTEM
- K113237 — CERTUS 140 2.45GHZ ABLATION SYSTEM
- K100744 — CERTUS 140 MICROWAVE ABLATION SYSTEM AND ACCESSORIES, MODEL CERTUS 140
Data sourced from openFDA. This site is unofficial and independent of the FDA.