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FDA 510(k), K980196, MD TECH BIOPSY SET FOR BONE AND BONE MARROW
FDA 510(k), K980196, MD TECH BIOPSY SET FOR BONE AND BONE MARROW
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510(K) Number: K980196
Device Name: MD TECH BIOPSY SET FOR BONE AND BONE MARROW
Manufacturer: MEDICAL DEVICE TECHNOLOGIES, INC.
Device Classification Name: instrument, biopsy
Regulation Number: 876.1075
Classification Product Code: KNW
Date Received: 01/20/1998
Decision Date: 02/03/1998
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: MD TECH BIOPSY SET FOR BONE AND BONE MARROW
Manufacturer: MEDICAL DEVICE TECHNOLOGIES, INC.
Device Classification Name: instrument, biopsy
Regulation Number: 876.1075
Classification Product Code: KNW
Date Received: 01/20/1998
Decision Date: 02/03/1998
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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