Neuron Therapeutics, Inc.
Country not established
- Devices
- 1
What Neuron Therapeutics, Inc. makes
Neuron Therapeutics, Inc. manufactures a 14-gauge lumbar puncture set, designed for spinal fluid access procedures.
The company’s products are regulated as Class II devices under FDA 510(k) clearance and are listed in the FDA registry.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuron Therapeutics, Inc. have in the registry?
The registry currently lists 1 device for Neuron Therapeutics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuron Therapeutics, Inc.'s devices?
Among its 1 most recently registered device, Neuron Therapeutics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neuron Therapeutics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neuron Therapeutics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuron Therapeutics, Inc. in the registry?
The most recently registered devices listed for Neuron Therapeutics, Inc. include NEURON THERAPEUTICS, INC., 14-GAUGE LUMBAR PUNCTURE SET, MODEL PN1000735.