Symbia Intevo Bold
K-Number: K162483 · 2017-01-09
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2017-01-09
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Symbia Intevo Bold is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2017-01-09 under approval number K162483. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Symbia Intevo Bold?
Symbia Intevo Bold is a medical device that received FDA 510(k) clearance on 2017-01-09. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K162483.
When was Symbia Intevo Bold approved by the FDA?
Symbia Intevo Bold received FDA 510(k) clearance on 2017-01-09, under approval number K162483.
What company makes Symbia Intevo Bold?
Symbia Intevo Bold is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for Symbia Intevo Bold?
The FDA product code for Symbia Intevo Bold is KPS.
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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.