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FDA 510(k)

R2 FAMILY OF IMAGE DISPLAY UNITS WITH R2 UNIFORM DISPLAY SOFTWARE

K-Number: K050667 · 2005-03-29

ApplicantR2 Technology, Inc.
Decision Date2005-03-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

R2 FAMILY OF IMAGE DISPLAY UNITS WITH R2 UNIFORM DISPLAY SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is R2 Technology, Inc.. It received FDA 510(k) clearance on 2005-03-29 under 510(k) number K050667. 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 R2 FAMILY OF IMAGE DISPLAY UNITS WITH R2 UNIFORM DISPLAY SOFTWARE?

R2 FAMILY OF IMAGE DISPLAY UNITS WITH R2 UNIFORM DISPLAY SOFTWARE is a medical device that received FDA 510(k) clearance on 2005-03-29. The listed applicant is R2 Technology, Inc.. The 510(k) number is K050667.

When did R2 FAMILY OF IMAGE DISPLAY UNITS WITH R2 UNIFORM DISPLAY SOFTWARE receive FDA 510(k) clearance?

R2 FAMILY OF IMAGE DISPLAY UNITS WITH R2 UNIFORM DISPLAY SOFTWARE received FDA 510(k) clearance on 2005-03-29, under 510(k) number K050667.

Who is the listed applicant for R2 FAMILY OF IMAGE DISPLAY UNITS WITH R2 UNIFORM DISPLAY SOFTWARE?

The FDA 510(k) record lists R2 Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for R2 FAMILY OF IMAGE DISPLAY UNITS WITH R2 UNIFORM DISPLAY SOFTWARE?

The FDA product code for R2 FAMILY OF IMAGE DISPLAY UNITS WITH R2 UNIFORM DISPLAY SOFTWARE is LLZ.

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Other records listing R2 Technology, Inc. as applicant

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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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