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FDA 510(k)

DBC, DONG BANG ACUPUNCTURE NEEDLES

K-Number: K990328 · 1999-05-04

ApplicantMorning Star, Dong Bang Acupuncture U.S.A., Inc.
Decision Date1999-05-04
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DBC, DONG BANG ACUPUNCTURE NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Morning Star, Dong Bang Acupuncture U.S.A., Inc.. It received FDA 510(k) clearance on 1999-05-04 under 510(k) number K990328. 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 DBC, DONG BANG ACUPUNCTURE NEEDLES?

DBC, DONG BANG ACUPUNCTURE NEEDLES is a medical device that received FDA 510(k) clearance on 1999-05-04. The listed applicant is Morning Star, Dong Bang Acupuncture U.S.A., Inc.. The 510(k) number is K990328.

When did DBC, DONG BANG ACUPUNCTURE NEEDLES receive FDA 510(k) clearance?

DBC, DONG BANG ACUPUNCTURE NEEDLES received FDA 510(k) clearance on 1999-05-04, under 510(k) number K990328.

Who is the listed applicant for DBC, DONG BANG ACUPUNCTURE NEEDLES?

The FDA 510(k) record lists Morning Star, Dong Bang Acupuncture U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DBC, DONG BANG ACUPUNCTURE NEEDLES?

The FDA product code for DBC, DONG BANG 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.

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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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