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FDA 510(k)

CLOCKMINI, MODEL DF301; CLOCKNAVI, MODEL DF311

K-Number: K023942 · 2003-02-24

ApplicantYamato Corp.
Decision Date2003-02-24
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CLOCKMINI, MODEL DF301; CLOCKNAVI, MODEL DF311 is the device name listed in this FDA 510(k) record. The listed applicant is Yamato Corp.. It received FDA 510(k) clearance on 2003-02-24 under 510(k) number K023942. The device is classified under product code MNW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLOCKMINI, MODEL DF301; CLOCKNAVI, MODEL DF311?

CLOCKMINI, MODEL DF301; CLOCKNAVI, MODEL DF311 is a medical device that received FDA 510(k) clearance on 2003-02-24. The listed applicant is Yamato Corp.. The 510(k) number is K023942.

When did CLOCKMINI, MODEL DF301; CLOCKNAVI, MODEL DF311 receive FDA 510(k) clearance?

CLOCKMINI, MODEL DF301; CLOCKNAVI, MODEL DF311 received FDA 510(k) clearance on 2003-02-24, under 510(k) number K023942.

Who is the listed applicant for CLOCKMINI, MODEL DF301; CLOCKNAVI, MODEL DF311?

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

What is the FDA product code for CLOCKMINI, MODEL DF301; CLOCKNAVI, MODEL DF311?

The FDA product code for CLOCKMINI, MODEL DF301; CLOCKNAVI, MODEL DF311 is MNW.

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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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