Symbia 6.7
K-Number: K200474 · 2020-03-20
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2020-03-20
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Symbia 6.7 is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2020-03-20 under approval number K200474. 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 6.7?
Symbia 6.7 is a medical device that received FDA 510(k) clearance on 2020-03-20. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K200474.
When was Symbia 6.7 approved by the FDA?
Symbia 6.7 received FDA 510(k) clearance on 2020-03-20, under approval number K200474.
What company makes Symbia 6.7?
Symbia 6.7 is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for Symbia 6.7?
The FDA product code for Symbia 6.7 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.