# K110606: MV Intradermic Needles; Magic Needle; Magic Needle

- Pathway: 510(k) (Traditional)
- Applicant: M.V.S.R.L.
- Decided: Sep 29, 2011 after 210 days
- Product code: FMI (Needle, Hypodermic, Single Lumen)
- Device class: 2
- Regulation: 21 CFR 880.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K051783 (2005). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051783: Artsana Pen Needles, Artsana Injection Needles, Artsana S.P.A (2005) Summary page 1.

## Most influential descendants
- K161255: meso-relle (AAL34, AAL36, AM30G) (2017), 1 descendant of its own
- K230070: MESORAM® Hypodermic Needle (710301); MESORAM® Hypodermic Needle (710302); MESORAM® Hypodermic Needle (712305); MESORAM® Hypodermic Needle (712315); MESORAM® Hypodermic Needle (710303); MESORAM® Hypodermic Needle (710307); MESORAM® Hypodermic Needle (710306); MESORAM® Hypodermic Needle (712308); MESORAM® Hypodermic Needle (712318); MESORAM® Hypodermic Needle (712303); MESORAM® Hypodermic Needle (712307); MESORAM® Hypodermic Needle (712306); MESORAM® Hypodermic Needle (812400); MESORAM® (2023), 0 descendants of its own

## Indications for use
The MV intraderniic needles are intended to inject fluids intradermally.

Source page: https://510kreport.com/device/K110606
Methodology: https://510kreport.com/methodology