Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) 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

Decision Date2022-11-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TorchTM Software is a medical device manufactured by Voximetry, Incorporated. It received FDA 510(k) clearance on 2022-11-28 under approval 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. It is manufactured by Voximetry, Incorporated. The 510(k) number is K220630.

When was TorchTM Software approved by the FDA?

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

What company makes TorchTM Software?

TorchTM Software is manufactured by Voximetry, Incorporated.

What is the FDA product code for TorchTM Software?

The FDA product code for TorchTM Software 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.