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FDA 510(k), K081532, PHARMAJET NEEDLE-FREE INJECTION SYSTEM
FDA 510(k), K081532, PHARMAJET NEEDLE-FREE INJECTION SYSTEM
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510(K) Number: K081532
Device Name: PHARMAJET 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: 06/02/2008
Decision Date: 02/26/2009
Regulation Medical Specialty: General Hospital
Device Name: PHARMAJET 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: 06/02/2008
Decision Date: 02/26/2009
Regulation Medical Specialty: General Hospital
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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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