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FDA 510(k)

CENTRICITY AW SUITE OPTION

K-Number: K061372 · 2006-05-30

ApplicantGe Healthcare Information Technologies
Decision Date2006-05-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CENTRICITY AW SUITE OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Ge Healthcare Information Technologies. It received FDA 510(k) clearance on 2006-05-30 under 510(k) number K061372. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRICITY AW SUITE OPTION?

CENTRICITY AW SUITE OPTION is a medical device that received FDA 510(k) clearance on 2006-05-30. The listed applicant is Ge Healthcare Information Technologies. The 510(k) number is K061372.

When did CENTRICITY AW SUITE OPTION receive FDA 510(k) clearance?

CENTRICITY AW SUITE OPTION received FDA 510(k) clearance on 2006-05-30, under 510(k) number K061372.

Who is the listed applicant for CENTRICITY AW SUITE OPTION?

The FDA 510(k) record lists Ge Healthcare Information Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTRICITY AW SUITE OPTION?

The FDA product code for CENTRICITY AW SUITE OPTION is LLZ.

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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.

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