Intl. Cancer Screening Laboratories, Inc.
Country not established
- Devices
- 1
What Intl. Cancer Screening Laboratories, Inc. makes
Intl. Cancer Screening Laboratories, Inc. produces the DIVERSI-KIT, a diagnostic device used for screening purposes in cancer detection.
The DIVERSI-KIT is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Diversi-Kit Ref K882485
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intl. Cancer Screening Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Intl. Cancer Screening Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intl. Cancer Screening Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Intl. Cancer Screening Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Intl. Cancer Screening Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intl. Cancer Screening Laboratories, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Intl. Cancer Screening Laboratories, Inc. in the registry?
The most recently registered devices listed for Intl. Cancer Screening Laboratories, Inc. include DIVERSI-KIT.