MICRO 2 HYPODERMIC NEEDLES

Needle, Hypodermic, Single Lumen

SMITH & NEPHEW, MPL DIVISION

The following data is part of a premarket notification filed by Smith & Nephew, Mpl Division with the FDA for Micro 2 Hypodermic Needles.

Pre-market Notification Details

Device IDK830242
510k NumberK830242
Device Name:MICRO 2 HYPODERMIC NEEDLES
ClassificationNeedle, Hypodermic, Single Lumen
Applicant SMITH & NEPHEW, MPL DIVISION 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFMI  
CFR Regulation Number880.5570 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-01-25
Decision Date1983-02-15

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