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FDA 510(k)

MILLENNIA ACUPUNCTURE NEEDLE

K-Number: K001718 · 2000-06-21

ApplicantUnited Pacific Co., Ltd.
Decision Date2000-06-21
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MILLENNIA ACUPUNCTURE NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is United Pacific Co., Ltd.. It received FDA 510(k) clearance on 2000-06-21 under 510(k) number K001718. 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 MILLENNIA ACUPUNCTURE NEEDLE?

MILLENNIA ACUPUNCTURE NEEDLE is a medical device that received FDA 510(k) clearance on 2000-06-21. The listed applicant is United Pacific Co., Ltd.. The 510(k) number is K001718.

When did MILLENNIA ACUPUNCTURE NEEDLE receive FDA 510(k) clearance?

MILLENNIA ACUPUNCTURE NEEDLE received FDA 510(k) clearance on 2000-06-21, under 510(k) number K001718.

Who is the listed applicant for MILLENNIA ACUPUNCTURE NEEDLE?

The FDA 510(k) record lists United Pacific Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MILLENNIA ACUPUNCTURE NEEDLE?

The FDA product code for MILLENNIA ACUPUNCTURE NEEDLE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing United Pacific Co., Ltd. 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.

K003010SPIRIT ACUPUNCTURE NEEDLEK993123QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2BK991503SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36K990406KINGLI ACUPUNCTURE NEEDLE

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.

K162566AIK Sterile Acupuncture Needles for Single UseChangchun Aik Medical Devices Co., Ltd.K132896CJ-TYPE: METAL HANDLE WITH GUIDE TUBE, PJ-TYPE: PLASTIC HANDLE WITH GUIDE TUBE, CB-TYPE: METAL HANDLE WITHOUT GUIDE TUBEAsia-Med GmbH and CO KGK111392WOOJEON ACUPUNCTURE NEEDLE (=SERA ACUPUNCTURE NEEDLE)Woojeon CompanyK103061BIOMATE STERILE ACUPUNCTURE NEEDLEBiomate Medical Devices Technology Co., Ltd.K092240ACUPUNCTURE NEEDLESHaenglim Seowon Medical Co.K090199JIAJIAN ACUPUNCTURE NEEDLEWuxi Jiajian Medical Instrument Co., Ltd.

Official Source

View on FDA Database →

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

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