Crown HT
K-Number: K242277 · 2024-10-01
ApplicantSprintray, Inc.
Decision Date2024-10-01
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Crown HT is a medical device manufactured by Sprintray, Inc.. It received FDA 510(k) clearance on 2024-10-01 under approval number K242277. 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 Crown HT?
Crown HT is a medical device that received FDA 510(k) clearance on 2024-10-01. It is manufactured by Sprintray, Inc.. The 510(k) number is K242277.
When was Crown HT approved by the FDA?
Crown HT received FDA 510(k) clearance on 2024-10-01, under approval number K242277.
What company makes Crown HT?
Crown HT is manufactured by Sprintray, Inc..
What is the FDA product code for Crown HT?
The FDA product code for Crown HT 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.