I misuratori Keto-Mojo sono certificati FDA?

Keto-Mojo meters sold in the U.S. are FDA-approved class II medical devices for the in vitro self-testing of glucose and ketone levels, and is suitable for testing for Type 1, Type 2, and gestational diabetes.

The meter is manufactured in an FDA-inspected and approved establishment that also conforms to ISO:9001 manufacturing practices. The meter also conforms to ISO 15197:2013 standards.

Here are more specifics, in case you’re interested:

• • Keto-Mojo TD-4279 FDA device listing number D126843
  • Keto-Check, Inc FDA registration number 10055466
  • Manufacturing facility FDA establishment registration number: 3004145393
  • All our inventory is stored in an FDA-registered warehouse in Savannah GA. Registration number 12631797414
  • Complete supply-chain custody is maintained throughout to assure you of genuine, quality products.

Learn more about the accuracy and reliability of Keto-Mojo meters.