Digital Crown
K-Number: K222623 · 2022-12-14
ApplicantSprintray, Inc.
Decision Date2022-12-14
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Digital Crown is a medical device manufactured by Sprintray, Inc.. It received FDA 510(k) clearance on 2022-12-14 under approval number K222623. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Digital Crown?
Digital Crown is a medical device that received FDA 510(k) clearance on 2022-12-14. It is manufactured by Sprintray, Inc.. The 510(k) number is K222623.
When was Digital Crown approved by the FDA?
Digital Crown received FDA 510(k) clearance on 2022-12-14, under approval number K222623.
What company makes Digital Crown?
Digital Crown is manufactured by Sprintray, Inc..
What is the FDA product code for Digital Crown?
The FDA product code for Digital Crown is EBF.
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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.