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FDA 510(k)

IN-ROOM MRC/ MAGNETOM VISION AND IMPACT SYSTEMS

K-Number: K962927 · 1996-09-25

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1996-09-25
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IN-ROOM MRC/ MAGNETOM VISION AND IMPACT SYSTEMS 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 1996-09-25 under 510(k) number K962927. 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 IN-ROOM MRC/ MAGNETOM VISION AND IMPACT SYSTEMS?

IN-ROOM MRC/ MAGNETOM VISION AND IMPACT SYSTEMS is a medical device that received FDA 510(k) clearance on 1996-09-25. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K962927.

When did IN-ROOM MRC/ MAGNETOM VISION AND IMPACT SYSTEMS receive FDA 510(k) clearance?

IN-ROOM MRC/ MAGNETOM VISION AND IMPACT SYSTEMS received FDA 510(k) clearance on 1996-09-25, under 510(k) number K962927.

Who is the listed applicant for IN-ROOM MRC/ MAGNETOM VISION AND IMPACT SYSTEMS?

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 IN-ROOM MRC/ MAGNETOM VISION AND IMPACT SYSTEMS?

The FDA product code for IN-ROOM MRC/ MAGNETOM VISION AND IMPACT SYSTEMS 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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