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FDA 510(k)

INTEGRA RADIONICS XKNIFE RT 4

K-Number: K061893 · 2006-07-25

ApplicantIntegra Radionics, Inc.
Decision Date2006-07-25
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTEGRA RADIONICS XKNIFE RT 4 is the device name listed in this FDA 510(k) record. The listed applicant is Integra Radionics, Inc.. It received FDA 510(k) clearance on 2006-07-25 under 510(k) number K061893. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTEGRA RADIONICS XKNIFE RT 4?

INTEGRA RADIONICS XKNIFE RT 4 is a medical device that received FDA 510(k) clearance on 2006-07-25. The listed applicant is Integra Radionics, Inc.. The 510(k) number is K061893.

When did INTEGRA RADIONICS XKNIFE RT 4 receive FDA 510(k) clearance?

INTEGRA RADIONICS XKNIFE RT 4 received FDA 510(k) clearance on 2006-07-25, under 510(k) number K061893.

Who is the listed applicant for INTEGRA RADIONICS XKNIFE RT 4?

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

What is the FDA product code for INTEGRA RADIONICS XKNIFE RT 4?

The FDA product code for INTEGRA RADIONICS XKNIFE RT 4 is MUJ.

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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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