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FDA 510(k)

MAGNETIC RESON DIAG DEVICE MAGNETOM PROJECT 016

K-Number: K932271 · 1994-01-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1994-01-07
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETIC RESON DIAG DEVICE MAGNETOM 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 1994-01-07 under 510(k) number K932271. 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 MAGNETIC RESON DIAG DEVICE MAGNETOM PROJECT 016?

MAGNETIC RESON DIAG DEVICE MAGNETOM PROJECT 016 is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K932271.

When did MAGNETIC RESON DIAG DEVICE MAGNETOM PROJECT 016 receive FDA 510(k) clearance?

MAGNETIC RESON DIAG DEVICE MAGNETOM PROJECT 016 received FDA 510(k) clearance on 1994-01-07, under 510(k) number K932271.

Who is the listed applicant for MAGNETIC RESON DIAG DEVICE MAGNETOM 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 MAGNETIC RESON DIAG DEVICE MAGNETOM PROJECT 016?

The FDA product code for MAGNETIC RESON DIAG DEVICE MAGNETOM 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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