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FDA 510(k)

SIREMOBILE C06

K-Number: K040066 · 2004-02-12

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2004-02-12
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIREMOBILE C06 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2004-02-12 under 510(k) number K040066. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIREMOBILE C06?

SIREMOBILE C06 is a medical device that received FDA 510(k) clearance on 2004-02-12. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K040066.

When did SIREMOBILE C06 receive FDA 510(k) clearance?

SIREMOBILE C06 received FDA 510(k) clearance on 2004-02-12, under 510(k) number K040066.

Who is the listed applicant for SIREMOBILE C06?

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

What is the FDA product code for SIREMOBILE C06?

The FDA product code for SIREMOBILE C06 is OXO.

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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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