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FDA 510(k)

GE SIGNA PROFILE 6 INCH GP COIL

K-Number: K041921 · 2004-07-26

ApplicantGe Medical Systems, LLC
Decision Date2004-07-26
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE SIGNA PROFILE 6 INCH GP COIL is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems, LLC. It received FDA 510(k) clearance on 2004-07-26 under 510(k) number K041921. 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 GE SIGNA PROFILE 6 INCH GP COIL?

GE SIGNA PROFILE 6 INCH GP COIL is a medical device that received FDA 510(k) clearance on 2004-07-26. The listed applicant is Ge Medical Systems, LLC. The 510(k) number is K041921.

When did GE SIGNA PROFILE 6 INCH GP COIL receive FDA 510(k) clearance?

GE SIGNA PROFILE 6 INCH GP COIL received FDA 510(k) clearance on 2004-07-26, under 510(k) number K041921.

Who is the listed applicant for GE SIGNA PROFILE 6 INCH GP COIL?

The FDA 510(k) record lists Ge Medical Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GE SIGNA PROFILE 6 INCH GP COIL?

The FDA product code for GE SIGNA PROFILE 6 INCH GP COIL 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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