EsCom250
K-Number: K231523 · 2023-07-24
ApplicantSpident Co., Ltd.
Decision Date2023-07-24
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
EsCom250 is a medical device manufactured by Spident Co., Ltd.. It received FDA 510(k) clearance on 2023-07-24 under approval number K231523. 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 EsCom250?
EsCom250 is a medical device that received FDA 510(k) clearance on 2023-07-24. It is manufactured by Spident Co., Ltd.. The 510(k) number is K231523.
When was EsCom250 approved by the FDA?
EsCom250 received FDA 510(k) clearance on 2023-07-24, under approval number K231523.
What company makes EsCom250?
EsCom250 is manufactured by Spident Co., Ltd..
What is the FDA product code for EsCom250?
The FDA product code for EsCom250 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.