Diagnocat
K-Number: K252934 · 2026-01-15
ApplicantDGNCT, LLC
Decision Date2026-01-15
Product CodeMYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Diagnocat is a medical device manufactured by DGNCT, LLC. It received FDA 510(k) clearance on 2026-01-15 under approval number K252934. The device is classified under product code MYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Diagnocat?
Diagnocat is a medical device that received FDA 510(k) clearance on 2026-01-15. It is manufactured by DGNCT, LLC. The 510(k) number is K252934.
When was Diagnocat approved by the FDA?
Diagnocat received FDA 510(k) clearance on 2026-01-15, under approval number K252934.
What company makes Diagnocat?
Diagnocat is manufactured by DGNCT, LLC.
What is the FDA product code for Diagnocat?
The FDA product code for Diagnocat is MYN.
Other Devices by DGNCT, LLC
Related Devices (Code: MYN)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.