Larkspur Consulting Co.
Country not established
- Devices
- 1
What Larkspur Consulting Co. makes
Larkspur Consulting Co. manufactures patient examination gloves, designed for single-use in clinical settings to reduce cross-contamination during medical procedures.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Patient Examination Glove Ref K892986
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Larkspur Consulting Co. have in the registry?
The registry currently lists 1 device for Larkspur Consulting Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Larkspur Consulting Co.'s devices?
Among its 1 most recently registered device, Larkspur Consulting Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Larkspur Consulting Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Larkspur Consulting Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Larkspur Consulting Co. in the registry?
The most recently registered devices listed for Larkspur Consulting Co. include PATIENT EXAMINATION GLOVE.