Herco Products, Inc.
Country not established
- Devices
- 1
What Herco Products, Inc. makes
Herco Products, Inc. manufactures the HERCO Silicone Resuscitator, a manual resuscitation device designed for use in emergency medical situations to provide positive-pressure ventilation to patients.
The company’s portfolio is regulated under FDA’s Class II device classification, with devices listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Herco Products, Inc. have in the registry?
The registry currently lists 1 device for Herco Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Herco Products, Inc.'s devices?
Among its 1 most recently registered device, Herco Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Herco Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Herco Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Herco Products, Inc. in the registry?
The most recently registered devices listed for Herco Products, Inc. include HERCO SILICONE RESUSCITATOR OR SUN-MED RESUSCITA..