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FDA 510(k)

ACUPUNCTURE NEEDLE PACK

K-Number: K960769 · 1996-07-10

ApplicantAcu-Med, Inc.
Decision Date1996-07-10
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACUPUNCTURE NEEDLE PACK is the device name listed in this FDA 510(k) record. The listed applicant is Acu-Med, Inc.. It received FDA 510(k) clearance on 1996-07-10 under 510(k) number K960769. 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 PACK?

ACUPUNCTURE NEEDLE PACK is a medical device that received FDA 510(k) clearance on 1996-07-10. The listed applicant is Acu-Med, Inc.. The 510(k) number is K960769.

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

ACUPUNCTURE NEEDLE PACK received FDA 510(k) clearance on 1996-07-10, under 510(k) number K960769.

Who is the listed applicant for ACUPUNCTURE NEEDLE PACK?

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

What is the FDA product code for ACUPUNCTURE NEEDLE PACK?

The FDA product code for ACUPUNCTURE NEEDLE PACK is MQX.

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Other records listing Acu-Med, 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.

K021321WRIST FUSION PLATEK013616POLARUS CAP SCREWK012655CONGRUENT BONE PLATE SYSTEMK992525ACUMED MODULAR SHOULDER SYSTEMK993657ACUMED SUTURE ANCHORK980103ACUMED SUTURE ANCHOR

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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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