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)

VicorderCS (VCS-SYS-1100)

K-Number: K260693 · 2026-06-16

Decision Date2026-06-16
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VicorderCS (VCS-SYS-1100) is the device name listed in this FDA 510(k) record. The listed applicant is 80 Beats Medical GmbH. It received FDA 510(k) clearance on 2026-06-16 under 510(k) number K260693. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VicorderCS (VCS-SYS-1100)?

VicorderCS (VCS-SYS-1100) is a medical device that received FDA 510(k) clearance on 2026-06-16. The listed applicant is 80 Beats Medical GmbH. The 510(k) number is K260693.

When did VicorderCS (VCS-SYS-1100) receive FDA 510(k) clearance?

VicorderCS (VCS-SYS-1100) received FDA 510(k) clearance on 2026-06-16, under 510(k) number K260693.

Who is the listed applicant for VicorderCS (VCS-SYS-1100)?

The FDA 510(k) record lists 80 Beats Medical GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VicorderCS (VCS-SYS-1100)?

The FDA product code for VicorderCS (VCS-SYS-1100) is DXN.

Related Clinical Trials

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: DXN)

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.