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FDA 510(k)

AXIOM SIRESKOP SD

K-Number: K051602 · 2005-07-07

ApplicantSiemens Medical Systems, Inc.
Decision Date2005-07-07
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AXIOM SIRESKOP SD is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Systems, Inc.. It received FDA 510(k) clearance on 2005-07-07 under 510(k) number K051602. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXIOM SIRESKOP SD?

AXIOM SIRESKOP SD is a medical device that received FDA 510(k) clearance on 2005-07-07. The listed applicant is Siemens Medical Systems, Inc.. The 510(k) number is K051602.

When did AXIOM SIRESKOP SD receive FDA 510(k) clearance?

AXIOM SIRESKOP SD received FDA 510(k) clearance on 2005-07-07, under 510(k) number K051602.

Who is the listed applicant for AXIOM SIRESKOP SD?

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

What is the FDA product code for AXIOM SIRESKOP SD?

The FDA product code for AXIOM SIRESKOP SD is JAA.

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Other records listing Siemens Medical Systems, Inc. as applicant

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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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