FDA product code MAO: Dna-Probe, Human Chromosome
MAO is the FDA product code for dna-probe, human chromosome. It is a Unclassified device, reviewed by the Pathology panel. Devices under MAO reach the market by 510(k); FDA lists no cleared 510(k)s for it. 1 PMA application cites this product code. FDA has posted 1 recall for MAO devices.
Classification
| Field | Value |
|---|---|
| Device name | Dna-Probe, Human Chromosome |
| Device class | Unclassified |
| Review panel | PA — Pathology |
| Medical specialty | Unknown |
| Premarket route | 510(k) |
Recalls for MAO devices
1 product recalls in 1 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2005-10-28.
Frequently asked questions
What is FDA product code MAO?
MAO is the FDA product code for dna-probe, human chromosome. It is a Unclassified device, reviewed by the Pathology panel.
What device class is MAO?
Unclassified. Typical premarket route: 510(k).
Have MAO devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2005-10-28.
Next steps
- Run an FDA pathway report with predicate devices for product code MAO
- Run a recall and safety report across every MAO manufacturer
- Watch product code MAO for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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