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FDA 510(k)

XIMATRON V

K-Number: K810858 · 1981-05-13

ApplicantSiemens Corp.
Decision Date1981-05-13
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XIMATRON V is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1981-05-13 under 510(k) number K810858. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XIMATRON V?

XIMATRON V is a medical device that received FDA 510(k) clearance on 1981-05-13. The listed applicant is Siemens Corp.. The 510(k) number is K810858.

When did XIMATRON V receive FDA 510(k) clearance?

XIMATRON V received FDA 510(k) clearance on 1981-05-13, under 510(k) number K810858.

Who is the listed applicant for XIMATRON V?

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

What is the FDA product code for XIMATRON V?

The FDA product code for XIMATRON V is KPQ.

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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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