FDA 510(k)

WebCeph

K-Number: K220903 · 2022-08-17

Decision Date2022-08-17

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

WebCeph is the device name listed in this FDA 510(k) record. The listed applicant is Assemblecircle Corp.. It received FDA 510(k) clearance on 2022-08-17 under 510(k) number K220903. 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 WebCeph?

WebCeph is a medical device that received FDA 510(k) clearance on 2022-08-17. The listed applicant is Assemblecircle Corp.. The 510(k) number is K220903.

When did WebCeph receive FDA 510(k) clearance?

WebCeph received FDA 510(k) clearance on 2022-08-17, under 510(k) number K220903.

Who is the listed applicant for WebCeph?

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

What is the FDA product code for WebCeph?

The FDA product code for WebCeph 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.