FDA 510(k), K100744, CERTUS 140 MICROWAVE ABLATION SYSTEM AND ACCESSORIES, MODEL CERTUS 140
FDA 510(k), K100744, CERTUS 140 MICROWAVE ABLATION SYSTEM AND ACCESSORIES, MODEL CERTUS 140
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510(K) Number: K100744
Device Name: CERTUS 140 MICROWAVE ABLATION SYSTEM AND ACCESSORIES, MODEL CERTUS 140
Manufacturer: NEUWAVE MEDICAL, INC
Device Classification Name: system, ablation, microwave and accessories
Regulation Number: 878.4400
Classification Product Code: NEY
Date Received: 03/16/2010
Decision Date: 10/22/2010
Regulation Medical Specialty: General & Plastic Surgery
Device Name: CERTUS 140 MICROWAVE ABLATION SYSTEM AND ACCESSORIES, MODEL CERTUS 140
Manufacturer: NEUWAVE MEDICAL, INC
Device Classification Name: system, ablation, microwave and accessories
Regulation Number: 878.4400
Classification Product Code: NEY
Date Received: 03/16/2010
Decision Date: 10/22/2010
Regulation Medical Specialty: General & Plastic Surgery
- 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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