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FDA 510(k), K904987, VIBRONICS AUTO CORE BIOPSY DEVICE (ACBD)
FDA 510(k), K904987, VIBRONICS AUTO CORE BIOPSY DEVICE (ACBD)
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510(K) Number: K904987
Device Name: VIBRONICS AUTO CORE BIOPSY DEVICE (ACBD)
Manufacturer: VIBRONICS
Device Classification Name: instrument, biopsy
Regulation Number: 876.1075
Classification Product Code: KNW
Date Received: 11/07/1990
Decision Date: 02/11/1991
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: VIBRONICS AUTO CORE BIOPSY DEVICE (ACBD)
Manufacturer: VIBRONICS
Device Classification Name: instrument, biopsy
Regulation Number: 876.1075
Classification Product Code: KNW
Date Received: 11/07/1990
Decision Date: 02/11/1991
Regulation Medical Specialty: Gastroenterology/Urology
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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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