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

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