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FDA 510(k), K030784, NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL
FDA 510(k), K030784, NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL
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510(K) Number: K030784
Device Name: NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL
Manufacturer: APPLIED MEDICAL TECHNOLOGY, INC.
Device Classification Name: Tubes, Gastrointestinal (And Accessories)
Regulation Number: 876.5980
Classification Product Code: KNT
Date Received: 03/12/2003
Decision Date: 04/01/2004
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL
Manufacturer: APPLIED MEDICAL TECHNOLOGY, INC.
Device Classification Name: Tubes, Gastrointestinal (And Accessories)
Regulation Number: 876.5980
Classification Product Code: KNT
Date Received: 03/12/2003
Decision Date: 04/01/2004
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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