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)

Elegant™ Advanced CompHort

K-Number: K231794 · 2023-12-22

Decision Date2023-12-22
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Elegant™ Advanced CompHort is the device name listed in this FDA 510(k) record. The listed applicant is Viramal Limited. It received FDA 510(k) clearance on 2023-12-22 under 510(k) number K231794. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Elegant™ Advanced CompHort?

Elegant™ Advanced CompHort is a medical device that received FDA 510(k) clearance on 2023-12-22. The listed applicant is Viramal Limited. The 510(k) number is K231794.

When did Elegant™ Advanced CompHort receive FDA 510(k) clearance?

Elegant™ Advanced CompHort received FDA 510(k) clearance on 2023-12-22, under 510(k) number K231794.

Who is the listed applicant for Elegant™ Advanced CompHort?

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

What is the FDA product code for Elegant™ Advanced CompHort?

The FDA product code for Elegant™ Advanced CompHort is NUC.

Other records listing Viramal Limited as applicant

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.

Related Devices (Code: NUC)

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.

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.