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FDA 510(k)

MODIFICATION TO: CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION

K-Number: K053356 · 2006-04-19

ApplicantGe Medical Systems Information Technologies
Decision Date2006-04-19
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO: CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION 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 2006-04-19 under 510(k) number K053356. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO: CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION?

MODIFICATION TO: CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION is a medical device that received FDA 510(k) clearance on 2006-04-19. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K053356.

When did MODIFICATION TO: CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION receive FDA 510(k) clearance?

MODIFICATION TO: CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION received FDA 510(k) clearance on 2006-04-19, under 510(k) number K053356.

Who is the listed applicant for MODIFICATION TO: CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION?

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 MODIFICATION TO: CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION?

The FDA product code for MODIFICATION TO: CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION is DXJ.

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Other records listing Ge Medical Systems Information Technologies as applicant

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Related Devices (Code: DXJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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