FDA product code NAZ: Stimulator, Bladder

NAZ is the FDA product code for stimulator, bladder. It is a HDE device, reviewed by the Gastroenterology and Urology panel. Devices under NAZ reach the market by Unclassified; FDA lists no cleared 510(k)s for it.

Classification

Recalls for NAZ devices

openFDA lists no recalls for product code NAZ.

Frequently asked questions

What is FDA product code NAZ?

NAZ is the FDA product code for stimulator, bladder. It is a HDE device, reviewed by the Gastroenterology and Urology panel.

What device class is NAZ?

HDE. Typical premarket route: Unclassified.

Next steps

• Run an FDA pathway report with predicate devices for product code NAZ
• Run a recall and safety report across every NAZ manufacturer
• Watch product code NAZ 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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