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FDA 510(k), K131249, ON-Q PAINBUSTER, ON-Q C-BLOC, HOMEPUMP ECLIPSE, HOMEPUMP C-SERIES
FDA 510(k), K131249, ON-Q PAINBUSTER, ON-Q C-BLOC, HOMEPUMP ECLIPSE, HOMEPUMP C-SERIES
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510(K) Number: K131249
Device Name: ON-Q PAINBUSTER, ON-Q C-BLOC, HOMEPUMP ECLIPSE, HOMEPUMP C-SERIES
Manufacturer: I-FLOW LLC
Device Classification Name: pump, infusion, elastomeric
Regulation Number: 880.5725
Classification Product Code: MEB
Date Received: 05/01/2013
Decision Date: 02/03/2014
Regulation Medical Specialty: General Hospital
Device Name: ON-Q PAINBUSTER, ON-Q C-BLOC, HOMEPUMP ECLIPSE, HOMEPUMP C-SERIES
Manufacturer: I-FLOW LLC
Device Classification Name: pump, infusion, elastomeric
Regulation Number: 880.5725
Classification Product Code: MEB
Date Received: 05/01/2013
Decision Date: 02/03/2014
Regulation Medical Specialty: General Hospital
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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