FDA 510(k), K771203, DISP. HYPODERMIC NEEDLE

FDA 510(k), K771203, DISP. HYPODERMIC NEEDLE

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510(K) Number: K771203
Device Name: DISP. HYPODERMIC NEEDLE
Manufacturer:
Device Classification Name: Needle, Hypodermic, Single Lumen
Regulation Number: FMI
Classification Product Code: KXA
Date Received: 07/05/1977
Decision Date: 07/14/1977
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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