Digital Temp
K-Number: K242559 · 2024-11-26
ApplicantSprintray, Inc.
Decision Date2024-11-26
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Digital Temp is a medical device manufactured by Sprintray, Inc.. It received FDA 510(k) clearance on 2024-11-26 under approval number K242559. 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 Digital Temp?
Digital Temp is a medical device that received FDA 510(k) clearance on 2024-11-26. It is manufactured by Sprintray, Inc.. The 510(k) number is K242559.
When was Digital Temp approved by the FDA?
Digital Temp received FDA 510(k) clearance on 2024-11-26, under approval number K242559.
What company makes Digital Temp?
Digital Temp is manufactured by Sprintray, Inc..
What is the FDA product code for Digital Temp?
The FDA product code for Digital Temp is EBG.
Other Devices by Sprintray, Inc.
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.