VERITON NM
K-Number: K180514 · 2018-04-25
Device Summary
Frequently Asked Questions
What is the VERITON NM?
VERITON NM is a medical device that received FDA 510(k) clearance on 2018-04-25. The listed applicant is Spectrum Dynamics Medical, Ltd.. The 510(k) number is K180514.
When did VERITON NM receive FDA 510(k) clearance?
VERITON NM received FDA 510(k) clearance on 2018-04-25, under 510(k) number K180514.
Who is the listed applicant for VERITON NM?
The FDA 510(k) record lists Spectrum Dynamics Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERITON NM?
The FDA product code for VERITON NM is KPS.
Other records listing Spectrum Dynamics Medical, Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KPS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.