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FDA 510(k)

SIENET COSMOS

K-Number: K033831 · 2003-12-19

ApplicantSiemens AG Medical Solutions
Decision Date2003-12-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIENET COSMOS is the device name listed in this FDA 510(k) record. The listed applicant is Siemens AG Medical Solutions. It received FDA 510(k) clearance on 2003-12-19 under 510(k) number K033831. 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 SIENET COSMOS?

SIENET COSMOS is a medical device that received FDA 510(k) clearance on 2003-12-19. The listed applicant is Siemens AG Medical Solutions. The 510(k) number is K033831.

When did SIENET COSMOS receive FDA 510(k) clearance?

SIENET COSMOS received FDA 510(k) clearance on 2003-12-19, under 510(k) number K033831.

Who is the listed applicant for SIENET COSMOS?

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

What is the FDA product code for SIENET COSMOS?

The FDA product code for SIENET COSMOS is LLZ.

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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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