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FDA 510(k), K092387, MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM
FDA 510(k), K092387, MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM
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510(K) Number: K092387
Device Name: MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM
Manufacturer: MINNTECH CORP.
Device Classification Name: accessories, cleaning, for endoscope
Regulation Number: 876.1500
Classification Product Code: FEB
Date Received: 08/05/2009
Decision Date: 04/05/2010
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEM
Manufacturer: MINNTECH CORP.
Device Classification Name: accessories, cleaning, for endoscope
Regulation Number: 876.1500
Classification Product Code: FEB
Date Received: 08/05/2009
Decision Date: 04/05/2010
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
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