FDA 510(k)

Augmented Reality Application

K-Number: K232339 · 2024-02-01

Decision Date2024-02-01

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Augmented Reality Application is the device name listed in this FDA 510(k) record. The listed applicant is Sira Medical, Inc.. It received FDA 510(k) clearance on 2024-02-01 under 510(k) number K232339. 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 Augmented Reality Application?

Augmented Reality Application is a medical device that received FDA 510(k) clearance on 2024-02-01. The listed applicant is Sira Medical, Inc.. The 510(k) number is K232339.

When did Augmented Reality Application receive FDA 510(k) clearance?

Augmented Reality Application received FDA 510(k) clearance on 2024-02-01, under 510(k) number K232339.

Who is the listed applicant for Augmented Reality Application?

The FDA 510(k) record lists Sira Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Augmented Reality Application?

The FDA product code for Augmented Reality Application 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.