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FDA 510(k)

MAGNETOM SYSTEMS WITH SYNGO EXPERT - I OPTION

K-Number: K052423 · 2006-01-13

ApplicantSiemens Medi Cal Solutions, Inc.
Decision Date2006-01-13
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAGNETOM SYSTEMS WITH SYNGO EXPERT - I OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medi Cal Solutions, Inc.. It received FDA 510(k) clearance on 2006-01-13 under 510(k) number K052423. 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 SYSTEMS WITH SYNGO EXPERT - I OPTION?

MAGNETOM SYSTEMS WITH SYNGO EXPERT - I OPTION is a medical device that received FDA 510(k) clearance on 2006-01-13. The listed applicant is Siemens Medi Cal Solutions, Inc.. The 510(k) number is K052423.

When did MAGNETOM SYSTEMS WITH SYNGO EXPERT - I OPTION receive FDA 510(k) clearance?

MAGNETOM SYSTEMS WITH SYNGO EXPERT - I OPTION received FDA 510(k) clearance on 2006-01-13, under 510(k) number K052423.

Who is the listed applicant for MAGNETOM SYSTEMS WITH SYNGO EXPERT - I OPTION?

The FDA 510(k) record lists Siemens Medi Cal Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGNETOM SYSTEMS WITH SYNGO EXPERT - I OPTION?

The FDA product code for MAGNETOM SYSTEMS WITH SYNGO EXPERT - I OPTION 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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