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FDA 510(k)

Z XT RADIATION THERAPY TREATMENT TABLE

K-Number: K910971 · 1991-05-03

ApplicantSiemens Medical Laboratories, Inc.
Decision Date1991-05-03
Product CodeJAI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Z XT RADIATION THERAPY TREATMENT TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1991-05-03 under 510(k) number K910971. The device is classified under product code JAI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Z XT RADIATION THERAPY TREATMENT TABLE?

Z XT RADIATION THERAPY TREATMENT TABLE is a medical device that received FDA 510(k) clearance on 1991-05-03. The listed applicant is Siemens Medical Laboratories, Inc.. The 510(k) number is K910971.

When did Z XT RADIATION THERAPY TREATMENT TABLE receive FDA 510(k) clearance?

Z XT RADIATION THERAPY TREATMENT TABLE received FDA 510(k) clearance on 1991-05-03, under 510(k) number K910971.

Who is the listed applicant for Z XT RADIATION THERAPY TREATMENT TABLE?

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

What is the FDA product code for Z XT RADIATION THERAPY TREATMENT TABLE?

The FDA product code for Z XT RADIATION THERAPY TREATMENT TABLE is JAI.

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Other records listing Siemens Medical Laboratories, Inc. as applicant

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Related Devices (Code: JAI)

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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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