Delta TT Pro
K-Number: K182099 · 2018-12-26
ApplicantLima Corporate S.P.A.
Decision Date2018-12-26
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Delta TT Pro is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2018-12-26 under approval number K182099. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Delta TT Pro?
Delta TT Pro is a medical device that received FDA 510(k) clearance on 2018-12-26. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K182099.
When was Delta TT Pro approved by the FDA?
Delta TT Pro received FDA 510(k) clearance on 2018-12-26, under approval number K182099.
What company makes Delta TT Pro?
Delta TT Pro is manufactured by Lima Corporate S.P.A..
What is the FDA product code for Delta TT Pro?
The FDA product code for Delta TT Pro is LPH.
Other Devices by Lima Corporate S.P.A.
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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.