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FDA 510(k), K110456, PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEM
FDA 510(k), K110456, PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEM
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510(K) Number: K110456
Device Name: PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEM
Manufacturer: PHARMAJET, INC.
Device Classification Name: Injector, Fluid, Non-Electrically Powered
Regulation Number: 880.5430
Classification Product Code: KZE
Date Received: 02/16/2011
Decision Date: 03/02/2011
Regulation Medical Specialty: General Hospital
Device Name: PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEM
Manufacturer: PHARMAJET, INC.
Device Classification Name: Injector, Fluid, Non-Electrically Powered
Regulation Number: 880.5430
Classification Product Code: KZE
Date Received: 02/16/2011
Decision Date: 03/02/2011
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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