Harold W. Berger Co.
Country not established
- Devices
- 1
What Harold W. Berger Co. makes
Harold W. Berger Co. manufactures the Laminaria Curex, a cervical dilator used in obstetric procedures to gradually widen the cervix prior to labor or surgical intervention.
The Laminaria Curex is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Laminaria Curex Ref K881295
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Harold W. Berger Co. have in the registry?
The registry currently lists 1 device for Harold W. Berger Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Harold W. Berger Co.'s devices?
Among its 1 most recently registered device, Harold W. Berger Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Harold W. Berger Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Harold W. Berger Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Harold W. Berger Co. in the registry?
The most recently registered devices listed for Harold W. Berger Co. include LAMINARIA CUREX.