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FDA 510(k), K041987, CORTRAK
FDA 510(k), K041987, CORTRAK
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510(K) Number: K041987
Device Name: CORTRAK
Manufacturer: VIASYS MEDSYSTEMS
Device Classification Name: tubes, gastrointestinal (and accessories)
Regulation Number: 876.5980
Classification Product Code: KNT
Date Received: 07/23/2004
Decision Date: 12/17/2004
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: CORTRAK
Manufacturer: VIASYS MEDSYSTEMS
Device Classification Name: tubes, gastrointestinal (and accessories)
Regulation Number: 876.5980
Classification Product Code: KNT
Date Received: 07/23/2004
Decision Date: 12/17/2004
Regulation Medical Specialty: Gastroenterology/Urology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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