CereMetrix Silver
K-Number: K173145 · 2018-02-28
ApplicantCeremetrix Corp
Decision Date2018-02-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
CereMetrix Silver is a medical device manufactured by Ceremetrix Corp. It received FDA 510(k) clearance on 2018-02-28 under approval number K173145. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CereMetrix Silver?
CereMetrix Silver is a medical device that received FDA 510(k) clearance on 2018-02-28. It is manufactured by Ceremetrix Corp. The 510(k) number is K173145.
When was CereMetrix Silver approved by the FDA?
CereMetrix Silver received FDA 510(k) clearance on 2018-02-28, under approval number K173145.
What company makes CereMetrix Silver?
CereMetrix Silver is manufactured by Ceremetrix Corp.
What is the FDA product code for CereMetrix Silver?
The FDA product code for CereMetrix Silver is LLZ.
Related Devices (Code: LLZ)
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.