SureSigns VS3; SureSigns VS4
K-Number: K163649 · 2017-03-31
ApplicantPhilips Medical Systems
Decision Date2017-03-31
Product CodeDSJ
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
SureSigns VS3; SureSigns VS4 is a medical device manufactured by Philips Medical Systems. It received FDA 510(k) clearance on 2017-03-31 under approval number K163649. The device is classified under product code DSJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SureSigns VS3; SureSigns VS4?
SureSigns VS3; SureSigns VS4 is a medical device that received FDA 510(k) clearance on 2017-03-31. It is manufactured by Philips Medical Systems. The 510(k) number is K163649.
When was SureSigns VS3; SureSigns VS4 approved by the FDA?
SureSigns VS3; SureSigns VS4 received FDA 510(k) clearance on 2017-03-31, under approval number K163649.
What company makes SureSigns VS3; SureSigns VS4?
SureSigns VS3; SureSigns VS4 is manufactured by Philips Medical Systems.
What is the FDA product code for SureSigns VS3; SureSigns VS4?
The FDA product code for SureSigns VS3; SureSigns VS4 is DSJ.
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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.