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FDA 510(k)

MAGNETOM VISION (PROJECT 016)

K-Number: K945779 · 1995-08-23

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1995-08-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETOM VISION (PROJECT 016) 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 1995-08-23 under 510(k) number K945779. 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 MAGNETOM VISION (PROJECT 016)?

MAGNETOM VISION (PROJECT 016) is a medical device that received FDA 510(k) clearance on 1995-08-23. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K945779.

When did MAGNETOM VISION (PROJECT 016) receive FDA 510(k) clearance?

MAGNETOM VISION (PROJECT 016) received FDA 510(k) clearance on 1995-08-23, under 510(k) number K945779.

Who is the listed applicant for MAGNETOM VISION (PROJECT 016)?

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 MAGNETOM VISION (PROJECT 016)?

The FDA product code for MAGNETOM VISION (PROJECT 016) 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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