MAOUnclassified

Dna-Probe, Human Chromosome

Unknown

MAO is the FDA product code for Dna-Probe, Human Chromosome. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code: MAO
Device name: Dna-Probe, Human Chromosome
Device class: Unclassified
Review panel: Unknown
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code MAO

FDA records hold no clearances under product code MAO.

Recent recalls

Product code MAO

Z-0416-06The DNA-Probe has a target size of ~300 Kb region instead of the labeled ~190 Kb region.Abbott Molecular / initiated 2005-10-28 / 749 kits

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)