FDA 510(k)

DINAMAP PROCARE SERIES MONITOR, MODELS 100N, 200N, 300N, 400N

K-Number: K022193 · 2002-08-01

ApplicantGe Medical Systems Information Technologies

Decision Date2002-08-01

Product CodeDQA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

DINAMAP PROCARE SERIES MONITOR, MODELS 100N, 200N, 300N, 400N 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 2002-08-01 under 510(k) number K022193. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DINAMAP PROCARE SERIES MONITOR, MODELS 100N, 200N, 300N, 400N?

DINAMAP PROCARE SERIES MONITOR, MODELS 100N, 200N, 300N, 400N is a medical device that received FDA 510(k) clearance on 2002-08-01. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K022193.

When did DINAMAP PROCARE SERIES MONITOR, MODELS 100N, 200N, 300N, 400N receive FDA 510(k) clearance?

DINAMAP PROCARE SERIES MONITOR, MODELS 100N, 200N, 300N, 400N received FDA 510(k) clearance on 2002-08-01, under 510(k) number K022193.

Who is the listed applicant for DINAMAP PROCARE SERIES MONITOR, MODELS 100N, 200N, 300N, 400N?

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 DINAMAP PROCARE SERIES MONITOR, MODELS 100N, 200N, 300N, 400N?

The FDA product code for DINAMAP PROCARE SERIES MONITOR, MODELS 100N, 200N, 300N, 400N is DQA.

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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.