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FDA 510(k)

DINAMAP PRO SERIES MONITOR, MODELS 110, 210, 310, 410

K-Number: K020022 · 2002-02-01

ApplicantGe Medical Systems Information Technologies
Decision Date2002-02-01
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DINAMAP PRO SERIES MONITOR, MODELS 110, 210, 310, 410 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 2002-02-01 under 510(k) number K020022. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DINAMAP PRO SERIES MONITOR, MODELS 110, 210, 310, 410?

DINAMAP PRO SERIES MONITOR, MODELS 110, 210, 310, 410 is a medical device that received FDA 510(k) clearance on 2002-02-01. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K020022.

When did DINAMAP PRO SERIES MONITOR, MODELS 110, 210, 310, 410 receive FDA 510(k) clearance?

DINAMAP PRO SERIES MONITOR, MODELS 110, 210, 310, 410 received FDA 510(k) clearance on 2002-02-01, under 510(k) number K020022.

Who is the listed applicant for DINAMAP PRO SERIES MONITOR, MODELS 110, 210, 310, 410?

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 PRO SERIES MONITOR, MODELS 110, 210, 310, 410?

The FDA product code for DINAMAP PRO SERIES MONITOR, MODELS 110, 210, 310, 410 is MWI.

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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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