DiaTemp Flow
K-Number: K192022 · 2020-02-13
ApplicantDiaDent Group International
Decision Date2020-02-13
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
DiaTemp Flow is a medical device manufactured by DiaDent Group International. It received FDA 510(k) clearance on 2020-02-13 under approval number K192022. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DiaTemp Flow?
DiaTemp Flow is a medical device that received FDA 510(k) clearance on 2020-02-13. It is manufactured by DiaDent Group International. The 510(k) number is K192022.
When was DiaTemp Flow approved by the FDA?
DiaTemp Flow received FDA 510(k) clearance on 2020-02-13, under approval number K192022.
What company makes DiaTemp Flow?
DiaTemp Flow is manufactured by DiaDent Group International.
What is the FDA product code for DiaTemp Flow?
The FDA product code for DiaTemp Flow is EBG.
Other Devices by DiaDent Group International
Related Devices (Code: EBG)
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.