Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TorchTM Software

K-Number: K220630 · 2022-11-28

ApplicantVoximetry, Incorporated
Decision Date2022-11-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TorchTM Software is the device name listed in this FDA 510(k) record. The listed applicant is Voximetry, Incorporated. It received FDA 510(k) clearance on 2022-11-28 under 510(k) number K220630. 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 TorchTM Software?

TorchTM Software is a medical device that received FDA 510(k) clearance on 2022-11-28. The listed applicant is Voximetry, Incorporated. The 510(k) number is K220630.

When did TorchTM Software receive FDA 510(k) clearance?

TorchTM Software received FDA 510(k) clearance on 2022-11-28, under 510(k) number K220630.

Who is the listed applicant for TorchTM Software?

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

What is the FDA product code for TorchTM Software?

The FDA product code for TorchTM Software 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, LLCK261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific CorporationK262143ImageGrid 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.

↑