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FDA 510(k)

SIEMENS MULTILEAF COLLIMATOR

K-Number: K953894 · 1995-11-13

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1995-11-13
Product CodeIXI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIEMENS MULTILEAF COLLIMATOR 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 1995-11-13 under 510(k) number K953894. The device is classified under product code IXI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS MULTILEAF COLLIMATOR?

SIEMENS MULTILEAF COLLIMATOR is a medical device that received FDA 510(k) clearance on 1995-11-13. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K953894.

When did SIEMENS MULTILEAF COLLIMATOR receive FDA 510(k) clearance?

SIEMENS MULTILEAF COLLIMATOR received FDA 510(k) clearance on 1995-11-13, under 510(k) number K953894.

Who is the listed applicant for SIEMENS MULTILEAF COLLIMATOR?

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 SIEMENS MULTILEAF COLLIMATOR?

The FDA product code for SIEMENS MULTILEAF COLLIMATOR is IXI.

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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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