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FDA 510(k)

ACUPUNCTURE NEEDLE UNDER THE BRAND NAME HWATO AND HUAXIA

K-Number: K974122 · 1998-01-22

Decision Date1998-01-22
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACUPUNCTURE NEEDLE UNDER THE BRAND NAME HWATO AND HUAXIA is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Health Care. It received FDA 510(k) clearance on 1998-01-22 under 510(k) number K974122. 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 ACUPUNCTURE NEEDLE UNDER THE BRAND NAME HWATO AND HUAXIA?

ACUPUNCTURE NEEDLE UNDER THE BRAND NAME HWATO AND HUAXIA is a medical device that received FDA 510(k) clearance on 1998-01-22. The listed applicant is Scientific Health Care. The 510(k) number is K974122.

When did ACUPUNCTURE NEEDLE UNDER THE BRAND NAME HWATO AND HUAXIA receive FDA 510(k) clearance?

ACUPUNCTURE NEEDLE UNDER THE BRAND NAME HWATO AND HUAXIA received FDA 510(k) clearance on 1998-01-22, under 510(k) number K974122.

Who is the listed applicant for ACUPUNCTURE NEEDLE UNDER THE BRAND NAME HWATO AND HUAXIA?

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

What is the FDA product code for ACUPUNCTURE NEEDLE UNDER THE BRAND NAME HWATO AND HUAXIA?

The FDA product code for ACUPUNCTURE NEEDLE UNDER THE BRAND NAME HWATO AND HUAXIA 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.

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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