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FDA 510(k)

SIEMENS BEAM SHAPER

K-Number: K961902 · 1996-08-08

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1996-08-08
Product CodeIXI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIEMENS BEAM SHAPER 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 1996-08-08 under 510(k) number K961902. 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 BEAM SHAPER?

SIEMENS BEAM SHAPER is a medical device that received FDA 510(k) clearance on 1996-08-08. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K961902.

When did SIEMENS BEAM SHAPER receive FDA 510(k) clearance?

SIEMENS BEAM SHAPER received FDA 510(k) clearance on 1996-08-08, under 510(k) number K961902.

Who is the listed applicant for SIEMENS BEAM SHAPER?

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 BEAM SHAPER?

The FDA product code for SIEMENS BEAM SHAPER 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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