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FDA 510(k)

FOX PULSE OXIMETER

K-Number: K051736 · 2005-12-02

Decision Date2005-12-02
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FOX PULSE OXIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Shunsuke Nakanishi. It received FDA 510(k) clearance on 2005-12-02 under 510(k) number K051736. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOX PULSE OXIMETER?

FOX PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 2005-12-02. The listed applicant is Shunsuke Nakanishi. The 510(k) number is K051736.

When did FOX PULSE OXIMETER receive FDA 510(k) clearance?

FOX PULSE OXIMETER received FDA 510(k) clearance on 2005-12-02, under 510(k) number K051736.

Who is the listed applicant for FOX PULSE OXIMETER?

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

What is the FDA product code for FOX PULSE OXIMETER?

The FDA product code for FOX PULSE OXIMETER is DQA.

Related Clinical Trials

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.

Related Devices (Code: DQA)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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