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FDA 510(k)

VOYAGER LINUX

K-Number: K023975 · 2002-12-20

ApplicantZ-Kat, Inc.
Decision Date2002-12-20
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VOYAGER LINUX is the device name listed in this FDA 510(k) record. The listed applicant is Z-Kat, Inc.. It received FDA 510(k) clearance on 2002-12-20 under 510(k) number K023975. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOYAGER LINUX?

VOYAGER LINUX is a medical device that received FDA 510(k) clearance on 2002-12-20. The listed applicant is Z-Kat, Inc.. The 510(k) number is K023975.

When did VOYAGER LINUX receive FDA 510(k) clearance?

VOYAGER LINUX received FDA 510(k) clearance on 2002-12-20, under 510(k) number K023975.

Who is the listed applicant for VOYAGER LINUX?

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

What is the FDA product code for VOYAGER LINUX?

The FDA product code for VOYAGER LINUX is HAW.

Related Clinical Trials

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Other records listing Z-Kat, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K030764Z-BOXK013025MODIFICATION TO FLOUROLAB PLUSK002893FLUOROLAB PLUSK984298Z KAT FLUROTACTIC GUIDANCE SYSTEM MKI

Related Devices (Code: HAW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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