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CERTUS 140 2.45GHZ ABLATION SYSTEM

510(k) Status
Cleared
Active Recalls
None
Manufacturer
Neuwave Medical, Inc.
Country of Origin

What it is

Specifications

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Regulatory

FDA 510(k) Clearance

K122217
Cleared 2012-01-02 · Substantially Equivalent
Applicant: Neuwave Medical, Inc.
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Reference

Instructions for Use & Documents

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