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FDA 510(k), K930041, VICROSAFE 6 AND VICROSAFE 12
FDA 510(k), K930041, VICROSAFE 6 AND VICROSAFE 12
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510(K) Number: K930041
Device Name: VICROSAFE 6 AND VICROSAFE 12
Manufacturer: BUFFALO FILTER CO., INC.
Device Classification Name: apparatus, exhaust, surgical
Regulation Number: 878.5070
Classification Product Code: FYD
Date Received: 01/05/1993
Decision Date: 11/03/1993
Regulation Medical Specialty: General & Plastic Surgery
Device Name: VICROSAFE 6 AND VICROSAFE 12
Manufacturer: BUFFALO FILTER CO., INC.
Device Classification Name: apparatus, exhaust, surgical
Regulation Number: 878.5070
Classification Product Code: FYD
Date Received: 01/05/1993
Decision Date: 11/03/1993
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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