deepLive
K-Number: K240610 · 2024-07-09
ApplicantDamae Medical
Decision Date2024-07-09
Product CodeNQQ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
deepLive is a medical device manufactured by Damae Medical. It received FDA 510(k) clearance on 2024-07-09 under approval number K240610. The device is classified under product code NQQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the deepLive?
deepLive is a medical device that received FDA 510(k) clearance on 2024-07-09. It is manufactured by Damae Medical. The 510(k) number is K240610.
When was deepLive approved by the FDA?
deepLive received FDA 510(k) clearance on 2024-07-09, under approval number K240610.
What company makes deepLive?
deepLive is manufactured by Damae Medical.
What is the FDA product code for deepLive?
The FDA product code for deepLive is NQQ.
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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.