Plastic Parts Corp.
Country not established
- Devices
- 1
What Plastic Parts Corp. makes
Plastic Parts Corp. manufactures the Goettinger Emergency Resuscitation Tube, a disposable airway device designed for use in emergency resuscitation procedures to facilitate ventilation in patients requiring immediate airway management.
The Goettinger Emergency Resuscitation Tube is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance database. The company is based in the United States.
Catalogue
Goettinger Emergency Resuscitation Tube Ref K892123
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Plastic Parts Corp. have in the registry?
The registry currently lists 1 device for Plastic Parts Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Plastic Parts Corp.'s devices?
Among its 1 most recently registered device, Plastic Parts Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Plastic Parts Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Plastic Parts Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Plastic Parts Corp. in the registry?
The most recently registered devices listed for Plastic Parts Corp. include GOETTINGER EMERGENCY RESUSCITATION TUBE.