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FDA 510(k), K142335, RapidVac Smoke Evacuator System
FDA 510(k), K142335, RapidVac Smoke Evacuator System
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510(K) Number: K142335
Device Name: RapidVac Smoke Evacuator System
Manufacturer: COVIDIEN
Device Classification Name: apparatus, exhaust, surgical
Regulation Number: 878.5070
Classification Product Code: FYD
Date Received: 08/21/2014
Decision Date: 01/14/2015
Regulation Medical Specialty: General & Plastic Surgery
Device Name: RapidVac Smoke Evacuator System
Manufacturer: COVIDIEN
Device Classification Name: apparatus, exhaust, surgical
Regulation Number: 878.5070
Classification Product Code: FYD
Date Received: 08/21/2014
Decision Date: 01/14/2015
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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