VERITON NM
K-Number: K180514 · 2018-04-25
ApplicantSpectrum Dynamics Medical, Ltd.
Decision Date2018-04-25
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
VERITON NM is a medical device manufactured by Spectrum Dynamics Medical, Ltd.. It received FDA 510(k) clearance on 2018-04-25 under approval number K180514. 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 VERITON NM?
VERITON NM is a medical device that received FDA 510(k) clearance on 2018-04-25. It is manufactured by Spectrum Dynamics Medical, Ltd.. The 510(k) number is K180514.
When was VERITON NM approved by the FDA?
VERITON NM received FDA 510(k) clearance on 2018-04-25, under approval number K180514.
What company makes VERITON NM?
VERITON NM is manufactured by Spectrum Dynamics Medical, Ltd..
What is the FDA product code for VERITON NM?
The FDA product code for VERITON NM 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.