Gresco International, Inc.
Country not established
- Devices
- 1
What Gresco International, Inc. makes
Gresco International, Inc. manufactures infant cannulas, which are tubular medical devices inserted into airways to facilitate breathing support for newborns and infants.
The company’s products are regulated as Class II devices under FDA requirements and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Infant Cannula Ref K873012
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gresco International, Inc. have in the registry?
The registry currently lists 1 device for Gresco International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gresco International, Inc.'s devices?
Among its 1 most recently registered device, Gresco International, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Gresco International, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gresco International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gresco International, Inc. in the registry?
The most recently registered devices listed for Gresco International, Inc. include INFANT CANNULA.