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FDA 510(k)

13C/1H OCCIPITAL HEADCOIL FOR MAGNETOM ALLEGRA

K-Number: K042718 · 2004-11-12

ApplicantSiemens Medi Cal Solutions, Inc.
Decision Date2004-11-12
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

13C/1H OCCIPITAL HEADCOIL FOR MAGNETOM ALLEGRA 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 2004-11-12 under 510(k) number K042718. 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 13C/1H OCCIPITAL HEADCOIL FOR MAGNETOM ALLEGRA?

13C/1H OCCIPITAL HEADCOIL FOR MAGNETOM ALLEGRA is a medical device that received FDA 510(k) clearance on 2004-11-12. The listed applicant is Siemens Medi Cal Solutions, Inc.. The 510(k) number is K042718.

When did 13C/1H OCCIPITAL HEADCOIL FOR MAGNETOM ALLEGRA receive FDA 510(k) clearance?

13C/1H OCCIPITAL HEADCOIL FOR MAGNETOM ALLEGRA received FDA 510(k) clearance on 2004-11-12, under 510(k) number K042718.

Who is the listed applicant for 13C/1H OCCIPITAL HEADCOIL FOR MAGNETOM ALLEGRA?

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 13C/1H OCCIPITAL HEADCOIL FOR MAGNETOM ALLEGRA?

The FDA product code for 13C/1H OCCIPITAL HEADCOIL FOR MAGNETOM ALLEGRA 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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