FDA 510(k), K092746, MICRONJET 600

FDA 510(k), K092746, MICRONJET 600

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510(K) Number: K092746
Device Name: MICRONJET 600
Manufacturer: JONATHAN KAHAN
Device Classification Name: Needle, Hypodermic, Single Lumen
Regulation Number: FMI
Classification Product Code: KXA
Date Received: 09/08/2009
Decision Date: 02/03/2010
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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