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FDA 510(k), K092172, EXEL I.V. EXTENSION SET
FDA 510(k), K092172, EXEL I.V. EXTENSION SET
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510(K) Number: K092172
Device Name: EXEL I.V. EXTENSION SET
Manufacturer: EXELINT INTL. CO.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 07/21/2009
Decision Date: 01/04/2010
Regulation Medical Specialty: General Hospital
Device Name: EXEL I.V. EXTENSION SET
Manufacturer: EXELINT INTL. CO.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 07/21/2009
Decision Date: 01/04/2010
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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