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FDA 510(k)

MAEDA NEW NEEDLE DISPOSABLE

K-Number: K000581 · 2001-02-23

Decision Date2001-02-23
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MAEDA NEW NEEDLE DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Maeda Toyokichi Shoten. It received FDA 510(k) clearance on 2001-02-23 under 510(k) number K000581. The device is classified under product code MQX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAEDA NEW NEEDLE DISPOSABLE?

MAEDA NEW NEEDLE DISPOSABLE is a medical device that received FDA 510(k) clearance on 2001-02-23. The listed applicant is Maeda Toyokichi Shoten. The 510(k) number is K000581.

When did MAEDA NEW NEEDLE DISPOSABLE receive FDA 510(k) clearance?

MAEDA NEW NEEDLE DISPOSABLE received FDA 510(k) clearance on 2001-02-23, under 510(k) number K000581.

Who is the listed applicant for MAEDA NEW NEEDLE DISPOSABLE?

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

What is the FDA product code for MAEDA NEW NEEDLE DISPOSABLE?

The FDA product code for MAEDA NEW NEEDLE DISPOSABLE is MQX.

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 Maeda Toyokichi Shoten 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: MQX)

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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