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FDA 510(k), K854593, NORFOLK MEDICAL PERITONEAL-ACCESS PORT
FDA 510(k), K854593, NORFOLK MEDICAL PERITONEAL-ACCESS PORT
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510(K) Number: K854593
Device Name: NORFOLK MEDICAL PERITONEAL-ACCESS PORT
Manufacturer: NORFOLK MEDICAL PRODUCTS, INC.
Device Classification Name: device, peritoneal access, subcutaneous, implanted
Regulation Number:
Classification Product Code: LMQ
Date Received: 11/18/1985
Decision Date: 02/04/1986
Regulation Medical Specialty:
Device Name: NORFOLK MEDICAL PERITONEAL-ACCESS PORT
Manufacturer: NORFOLK MEDICAL PRODUCTS, INC.
Device Classification Name: device, peritoneal access, subcutaneous, implanted
Regulation Number:
Classification Product Code: LMQ
Date Received: 11/18/1985
Decision Date: 02/04/1986
Regulation Medical Specialty:
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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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