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FDA 510(k)

AUXILIARY PATIENT TABLE/MAGNETOM OPEN SYSTEM

K-Number: K955811 · 1996-03-29

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1996-03-29
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AUXILIARY PATIENT TABLE/MAGNETOM OPEN SYSTEM 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 1996-03-29 under 510(k) number K955811. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUXILIARY PATIENT TABLE/MAGNETOM OPEN SYSTEM?

AUXILIARY PATIENT TABLE/MAGNETOM OPEN SYSTEM is a medical device that received FDA 510(k) clearance on 1996-03-29. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K955811.

When did AUXILIARY PATIENT TABLE/MAGNETOM OPEN SYSTEM receive FDA 510(k) clearance?

AUXILIARY PATIENT TABLE/MAGNETOM OPEN SYSTEM received FDA 510(k) clearance on 1996-03-29, under 510(k) number K955811.

Who is the listed applicant for AUXILIARY PATIENT TABLE/MAGNETOM OPEN SYSTEM?

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 AUXILIARY PATIENT TABLE/MAGNETOM OPEN SYSTEM?

The FDA product code for AUXILIARY PATIENT TABLE/MAGNETOM OPEN SYSTEM is LNH.

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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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