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FDA 510(k)

MODIFICATION TO CIC PRO CLINICAL INFORMATION CENTER

K-Number: K062976 · 2007-03-16

Decision Date2007-03-16
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO CIC PRO CLINICAL INFORMATION CENTER 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 2007-03-16 under 510(k) number K062976. 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 MODIFICATION TO CIC PRO CLINICAL INFORMATION CENTER?

MODIFICATION TO CIC PRO CLINICAL INFORMATION CENTER is a medical device that received FDA 510(k) clearance on 2007-03-16. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K062976.

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

MODIFICATION TO CIC PRO CLINICAL INFORMATION CENTER received FDA 510(k) clearance on 2007-03-16, under 510(k) number K062976.

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

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?

The FDA product code for MODIFICATION TO CIC PRO CLINICAL INFORMATION CENTER is DSI.

Related Clinical Trials

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.

Other records listing Ge Medical Systems Information Technologies as applicant

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.

View all 136 devices →

Related Devices (Code: DSI)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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