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FDA 510(k)

NAVIGATOR

K-Number: K042875 · 2005-07-01

ApplicantNomos Corp.
Decision Date2005-07-01
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NAVIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Nomos Corp.. It received FDA 510(k) clearance on 2005-07-01 under 510(k) number K042875. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAVIGATOR?

NAVIGATOR is a medical device that received FDA 510(k) clearance on 2005-07-01. The listed applicant is Nomos Corp.. The 510(k) number is K042875.

When did NAVIGATOR receive FDA 510(k) clearance?

NAVIGATOR received FDA 510(k) clearance on 2005-07-01, under 510(k) number K042875.

Who is the listed applicant for NAVIGATOR?

The FDA 510(k) record lists Nomos Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NAVIGATOR?

The FDA product code for NAVIGATOR is IYE.

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Other records listing Nomos Corp. as applicant

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K070611BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6K060895NOMOSSTAT, VERSION 1.0K032209NOMOS CORVUS 5.0MK013036NOMOS MOTORIZED CRANE IIK993675PEREGRINE RADIATION THERAPY DOSE CALCULATION SYSTEMK993359RAPTOR TREATMENT PLANNING SYSTEM

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Related Devices (Code: IYE)

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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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