CE Deliver (DLV)
K-Number: K252480 · 2025-12-19
ApplicantCapsoVision, Inc.
Decision Date2025-12-19
Product CodeNEZ
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
CE Deliver (DLV) is a medical device manufactured by CapsoVision, Inc.. It received FDA 510(k) clearance on 2025-12-19 under approval number K252480. The device is classified under product code NEZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CE Deliver (DLV)?
CE Deliver (DLV) is a medical device that received FDA 510(k) clearance on 2025-12-19. It is manufactured by CapsoVision, Inc.. The 510(k) number is K252480.
When was CE Deliver (DLV) approved by the FDA?
CE Deliver (DLV) received FDA 510(k) clearance on 2025-12-19, under approval number K252480.
What company makes CE Deliver (DLV)?
CE Deliver (DLV) is manufactured by CapsoVision, Inc..
What is the FDA product code for CE Deliver (DLV)?
The FDA product code for CE Deliver (DLV) is NEZ.
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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.