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FDA 510(k)

ACUPUNCTURE NEEDLES

K-Number: K970574 · 1997-04-24

ApplicantC.A.I. Industries Corp.
Decision Date1997-04-24
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACUPUNCTURE NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is C.A.I. Industries Corp.. It received FDA 510(k) clearance on 1997-04-24 under 510(k) number K970574. 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 NEEDLES?

ACUPUNCTURE NEEDLES is a medical device that received FDA 510(k) clearance on 1997-04-24. The listed applicant is C.A.I. Industries Corp.. The 510(k) number is K970574.

When did ACUPUNCTURE NEEDLES receive FDA 510(k) clearance?

ACUPUNCTURE NEEDLES received FDA 510(k) clearance on 1997-04-24, under 510(k) number K970574.

Who is the listed applicant for ACUPUNCTURE NEEDLES?

The FDA 510(k) record lists C.A.I. Industries Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACUPUNCTURE NEEDLES?

The FDA product code for 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.

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 C.A.I. Industries Corp. 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.

K041652ACUPUNCTURE NEEDLESK954577WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS

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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