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FDA 510(k)

CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION

K-Number: K032370 · 2003-08-13

ApplicantGe Medical Systems Information Technologies
Decision Date2003-08-13
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

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 2003-08-13 under 510(k) number K032370. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION?

CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION is a medical device that received FDA 510(k) clearance on 2003-08-13. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K032370.

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

CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION received FDA 510(k) clearance on 2003-08-13, under 510(k) number K032370.

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

The FDA product code for CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION is DSI.

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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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