FDA 510(k)

CereMetrix Silver

K-Number: K173145 · 2018-02-28

Decision Date2018-02-28

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CereMetrix Silver is the device name listed in this FDA 510(k) record. The listed applicant is Ceremetrix Corp. It received FDA 510(k) clearance on 2018-02-28 under 510(k) 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. The listed applicant is Ceremetrix Corp. The 510(k) number is K173145.

When did CereMetrix Silver receive FDA 510(k) clearance?

CereMetrix Silver received FDA 510(k) clearance on 2018-02-28, under 510(k) number K173145.

Who is the listed applicant for CereMetrix Silver?

The FDA 510(k) record lists Ceremetrix Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CereMetrix Silver?

The FDA product code for CereMetrix Silver is LLZ.

Related Devices (Code: LLZ)

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.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLC K261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific Corporation K262143ImageGrid StreamVueCandelis, Inc.

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.