Hemolaser Corp.
Country not established
- Devices
- 1
What Hemolaser Corp. makes
Hemolaser Corp. manufactures the HEMOLASER HEMOSCOPE, a device designed for examining blood and blood components under a microscope, typically used in hematology diagnostics.
The HEMOLASER HEMOSCOPE is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Hemolaser Hemoscope Ref K893816
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hemolaser Corp. have in the registry?
The registry currently lists 1 device for Hemolaser Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hemolaser Corp.'s devices?
Among its 1 most recently registered device, Hemolaser Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Hemolaser Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hemolaser Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hemolaser Corp. in the registry?
The most recently registered devices listed for Hemolaser Corp. include HEMOLASER HEMOSCOPE.