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FDA 510(k)

14-CHANNEL EXTREMITY COIL FOR MAGNETOM ESSENZA

K-Number: K100141 · 2010-08-27

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2010-08-27
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

14-CHANNEL EXTREMITY COIL FOR MAGNETOM ESSENZA 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 2010-08-27 under 510(k) number K100141. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 14-CHANNEL EXTREMITY COIL FOR MAGNETOM ESSENZA?

14-CHANNEL EXTREMITY COIL FOR MAGNETOM ESSENZA is a medical device that received FDA 510(k) clearance on 2010-08-27. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K100141.

When did 14-CHANNEL EXTREMITY COIL FOR MAGNETOM ESSENZA receive FDA 510(k) clearance?

14-CHANNEL EXTREMITY COIL FOR MAGNETOM ESSENZA received FDA 510(k) clearance on 2010-08-27, under 510(k) number K100141.

Who is the listed applicant for 14-CHANNEL EXTREMITY COIL FOR MAGNETOM ESSENZA?

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 14-CHANNEL EXTREMITY COIL FOR MAGNETOM ESSENZA?

The FDA product code for 14-CHANNEL EXTREMITY COIL FOR MAGNETOM ESSENZA is MOS.

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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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