FDA product code JMQ: M. Lysodeikticus Cells (Spectrophotometric), Lysozyme (Muramidase)
JMQ is the FDA product code for m. lysodeikticus cells (spectrophotometric), lysozyme (muramidase). It is a Class I device, regulated under 21 CFR 862.1490 and reviewed by the Clinical Chemistry panel. Devices under JMQ reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | M. Lysodeikticus Cells (Spectrophotometric), Lysozyme (Muramidase) |
| Device class | Class I |
| Regulation | 21 CFR 862.1490 |
| Review panel | CH — Clinical Chemistry |
| Medical specialty | Clinical Chemistry |
| Premarket route | 510(k) exempt |
Recalls for JMQ devices
openFDA lists no recalls for product code JMQ.
Frequently asked questions
What is FDA product code JMQ?
JMQ is the FDA product code for m. lysodeikticus cells (spectrophotometric), lysozyme (muramidase). It is a Class I device, regulated under 21 CFR 862.1490 and reviewed by the Clinical Chemistry panel.
What device class is JMQ?
Class I, regulation 21 CFR 862.1490. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code JMQ
- Run a recall and safety report across every JMQ manufacturer
- Watch product code JMQ 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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