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FDA 510(k)

NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES

K-Number: K031060 · 2003-07-11

Decision Date2003-07-11
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Lhasa Medical, Inc.. It received FDA 510(k) clearance on 2003-07-11 under 510(k) number K031060. 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 NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES?

NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES is a medical device that received FDA 510(k) clearance on 2003-07-11. The listed applicant is Lhasa Medical, Inc.. The 510(k) number is K031060.

When did NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES receive FDA 510(k) clearance?

NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES received FDA 510(k) clearance on 2003-07-11, under 510(k) number K031060.

Who is the listed applicant for NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES?

The FDA 510(k) record lists Lhasa Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES?

The FDA product code for NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES 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 Lhasa Medical, Inc. 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.

View all 11 devices →

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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