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FDA 510(k)

FX-2 NMS (2CHANNEL TABLE MODEL)

K-Number: K945509 · 1995-05-02

ApplicantFx-2
Decision Date1995-05-02
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FX-2 NMS (2CHANNEL TABLE MODEL) is the device name listed in this FDA 510(k) record. The listed applicant is Fx-2. It received FDA 510(k) clearance on 1995-05-02 under 510(k) number K945509. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FX-2 NMS (2CHANNEL TABLE MODEL)?

FX-2 NMS (2CHANNEL TABLE MODEL) is a medical device that received FDA 510(k) clearance on 1995-05-02. The listed applicant is Fx-2. The 510(k) number is K945509.

When did FX-2 NMS (2CHANNEL TABLE MODEL) receive FDA 510(k) clearance?

FX-2 NMS (2CHANNEL TABLE MODEL) received FDA 510(k) clearance on 1995-05-02, under 510(k) number K945509.

Who is the listed applicant for FX-2 NMS (2CHANNEL TABLE MODEL)?

The FDA 510(k) record lists Fx-2 as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FX-2 NMS (2CHANNEL TABLE MODEL)?

The FDA product code for FX-2 NMS (2CHANNEL TABLE MODEL) is IPF.

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.

Other records listing Fx-2 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.

Related Devices (Code: IPF)

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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