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FDA 510(k), K924732, PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM
FDA 510(k), K924732, PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM
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510(K) Number: K924732
Device Name: PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM
Manufacturer: BUFFALO FILTER CO., INC.
Device Classification Name: apparatus, exhaust, surgical
Regulation Number: 878.5070
Classification Product Code: FYD
Date Received: 09/22/1992
Decision Date: 09/13/1993
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM
Manufacturer: BUFFALO FILTER CO., INC.
Device Classification Name: apparatus, exhaust, surgical
Regulation Number: 878.5070
Classification Product Code: FYD
Date Received: 09/22/1992
Decision Date: 09/13/1993
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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