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FDA 510(k)

TIANXIE

K-Number: K003748 · 2001-01-26

ApplicantSuzhou Tianyi Acupuncture Instruments Co., Ltd.
Decision Date2001-01-26
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TIANXIE is the device name listed in this FDA 510(k) record. The listed applicant is Suzhou Tianyi Acupuncture Instruments Co., Ltd.. It received FDA 510(k) clearance on 2001-01-26 under 510(k) number K003748. 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 TIANXIE?

TIANXIE is a medical device that received FDA 510(k) clearance on 2001-01-26. The listed applicant is Suzhou Tianyi Acupuncture Instruments Co., Ltd.. The 510(k) number is K003748.

When did TIANXIE receive FDA 510(k) clearance?

TIANXIE received FDA 510(k) clearance on 2001-01-26, under 510(k) number K003748.

Who is the listed applicant for TIANXIE?

The FDA 510(k) record lists Suzhou Tianyi Acupuncture Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TIANXIE?

The FDA product code for TIANXIE is MQX.

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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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