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FDA 510(k), K122217, CERTUS 140 2.45GHZ ABLATION SYSTEM
FDA 510(k), K122217, CERTUS 140 2.45GHZ ABLATION SYSTEM
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510(K) Number: K122217
Device Name: CERTUS 140 2.45GHZ ABLATION SYSTEM
Manufacturer: NEUWAVE MEDICAL, INC
Device Classification Name: system, ablation, microwave and accessories
Regulation Number: 878.4400
Classification Product Code: NEY
Date Received: 07/25/2012
Decision Date: 12/19/2012
Regulation Medical Specialty: General & Plastic Surgery
Device Name: CERTUS 140 2.45GHZ ABLATION SYSTEM
Manufacturer: NEUWAVE MEDICAL, INC
Device Classification Name: system, ablation, microwave and accessories
Regulation Number: 878.4400
Classification Product Code: NEY
Date Received: 07/25/2012
Decision Date: 12/19/2012
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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