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FDA 510(k)

ARGUS, MODEL LCM

K-Number: K053207 · 2006-05-19

ApplicantSchiller AG
Decision Date2006-05-19
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARGUS, MODEL LCM is the device name listed in this FDA 510(k) record. The listed applicant is Schiller AG. It received FDA 510(k) clearance on 2006-05-19 under 510(k) number K053207. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGUS, MODEL LCM?

ARGUS, MODEL LCM is a medical device that received FDA 510(k) clearance on 2006-05-19. The listed applicant is Schiller AG. The 510(k) number is K053207.

When did ARGUS, MODEL LCM receive FDA 510(k) clearance?

ARGUS, MODEL LCM received FDA 510(k) clearance on 2006-05-19, under 510(k) number K053207.

Who is the listed applicant for ARGUS, MODEL LCM?

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

What is the FDA product code for ARGUS, MODEL LCM?

The FDA product code for ARGUS, MODEL LCM is MHX.

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Other records listing Schiller AG as applicant

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Related Devices (Code: MHX)

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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.

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