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FDA 510(k), K882295, FILLING VOLUME OPTION
FDA 510(k), K882295, FILLING VOLUME OPTION
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510(K) Number: K882295
Device Name: FILLING VOLUME OPTION
Manufacturer: ERIS MEDICAL TECHNOLOGY
Device Classification Name: system, irrigation, urological
Regulation Number: 876.5130
Classification Product Code: LJH
Date Received: 06/02/1988
Decision Date: 09/13/1988
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: FILLING VOLUME OPTION
Manufacturer: ERIS MEDICAL TECHNOLOGY
Device Classification Name: system, irrigation, urological
Regulation Number: 876.5130
Classification Product Code: LJH
Date Received: 06/02/1988
Decision Date: 09/13/1988
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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