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FDA 510(k)

SEER MC

K-Number: K042782 · 2005-09-02

ApplicantGe Medical Systems Information Technologies
Decision Date2005-09-02
Product CodeMLO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SEER MC is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Information Technologies. It received FDA 510(k) clearance on 2005-09-02 under 510(k) number K042782. The device is classified under product code MLO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEER MC?

SEER MC is a medical device that received FDA 510(k) clearance on 2005-09-02. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K042782.

When did SEER MC receive FDA 510(k) clearance?

SEER MC received FDA 510(k) clearance on 2005-09-02, under 510(k) number K042782.

Who is the listed applicant for SEER MC?

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

What is the FDA product code for SEER MC?

The FDA product code for SEER MC is MLO.

Other records listing Ge Medical Systems Information Technologies as applicant

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Related Devices (Code: MLO)

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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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