TechCare Trauma
K-Number: K242171 · 2025-01-17
ApplicantMilvue
Decision Date2025-01-17
Product CodeQBS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
TechCare Trauma is a medical device manufactured by Milvue. It received FDA 510(k) clearance on 2025-01-17 under approval number K242171. The device is classified under product code QBS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the TechCare Trauma?
TechCare Trauma is a medical device that received FDA 510(k) clearance on 2025-01-17. It is manufactured by Milvue. The 510(k) number is K242171.
When was TechCare Trauma approved by the FDA?
TechCare Trauma received FDA 510(k) clearance on 2025-01-17, under approval number K242171.
What company makes TechCare Trauma?
TechCare Trauma is manufactured by Milvue.
What is the FDA product code for TechCare Trauma?
The FDA product code for TechCare Trauma is QBS.
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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.