FDA product code HAS: Needle, Neurosurgical Suture
HAS is the FDA product code for needle, neurosurgical suture. It is a Class I device, regulated under 21 CFR 882.4650 and reviewed by the Neurology panel. Devices under HAS reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Needle, Neurosurgical Suture |
| Device class | Class I |
| Regulation | 21 CFR 882.4650 |
| Review panel | NE — Neurology |
| Medical specialty | Neurology |
| Premarket route | 510(k) exempt |
Recalls for HAS devices
openFDA lists no recalls for product code HAS.
Frequently asked questions
What is FDA product code HAS?
HAS is the FDA product code for needle, neurosurgical suture. It is a Class I device, regulated under 21 CFR 882.4650 and reviewed by the Neurology panel.
What device class is HAS?
Class I, regulation 21 CFR 882.4650. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code HAS
- Run a recall and safety report across every HAS manufacturer
- Watch product code HAS 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.