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FDA 510(k)

MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF)

K-Number: K940541 · 1994-11-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1994-11-07
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF) 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 1994-11-07 under 510(k) number K940541. 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 RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF)?

MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF) is a medical device that received FDA 510(k) clearance on 1994-11-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K940541.

When did MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF) receive FDA 510(k) clearance?

MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF) received FDA 510(k) clearance on 1994-11-07, under 510(k) number K940541.

Who is the listed applicant for MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF)?

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 RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF)?

The FDA product code for MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF) 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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