FDA 510(k)

GE MARQUETTE PRISM INFORMATION SERVER APPLICATIONS

K-Number: K001268 · 2000-07-17

ApplicantGeneral Electric Medical Systems Information Techn

Decision Date2000-07-17

Product CodeMHX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

GE MARQUETTE PRISM INFORMATION SERVER APPLICATIONS is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Medical Systems Information Techn. It received FDA 510(k) clearance on 2000-07-17 under 510(k) number K001268. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GE MARQUETTE PRISM INFORMATION SERVER APPLICATIONS?

GE MARQUETTE PRISM INFORMATION SERVER APPLICATIONS is a medical device that received FDA 510(k) clearance on 2000-07-17. The listed applicant is General Electric Medical Systems Information Techn. The 510(k) number is K001268.

When did GE MARQUETTE PRISM INFORMATION SERVER APPLICATIONS receive FDA 510(k) clearance?

GE MARQUETTE PRISM INFORMATION SERVER APPLICATIONS received FDA 510(k) clearance on 2000-07-17, under 510(k) number K001268.

Who is the listed applicant for GE MARQUETTE PRISM INFORMATION SERVER APPLICATIONS?

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

What is the FDA product code for GE MARQUETTE PRISM INFORMATION SERVER APPLICATIONS?

The FDA product code for GE MARQUETTE PRISM INFORMATION SERVER APPLICATIONS is MHX.

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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.