FDA product code MZF: Test, Hiv Detection
MZF is the FDA product code for test, hiv detection. It is a Class II device, regulated under 21 CFR 866.3956 and reviewed by the Microbiology panel. Devices under MZF reach the market by 510(k); FDA lists no cleared 510(k)s for it. FDA has posted 1 recall for MZF devices, 1 initiated in the last five years.
Classification
| Field | Value |
|---|---|
| Device name | Test, Hiv Detection |
| Device class | Class II |
| Regulation | 21 CFR 866.3956 |
| Review panel | MI — Microbiology |
| Medical specialty | Microbiology |
| Premarket route | 510(k) |
Recalls for MZF devices
1 product recalls in 1 recall events; 1 initiated in the last five years and 1 still open. Most recent: 2025-04-24.
| Year | Recalls |
|---|---|
| 2025 | 1 |
Frequently asked questions
What is FDA product code MZF?
MZF is the FDA product code for test, hiv detection. It is a Class II device, regulated under 21 CFR 866.3956 and reviewed by the Microbiology panel.
What device class is MZF?
Class II, regulation 21 CFR 866.3956. Typical premarket route: 510(k).
Have MZF devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2025-04-24.
Next steps
- Run an FDA pathway report with predicate devices for product code MZF
- Run a recall and safety report across every MZF manufacturer
- Watch product code MZF 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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