TAKI DISPOSABLE ACUPUNCTURE NEEDLE
K-Number: K962787 · 1996-07-26
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Device Summary
Frequently Asked Questions
What is the TAKI DISPOSABLE ACUPUNCTURE NEEDLE?
TAKI DISPOSABLE ACUPUNCTURE NEEDLE is a medical device that received FDA 510(k) clearance on 1996-07-26. The listed applicant is Acupuncture Supplies Import Co.. The 510(k) number is K962787.
When did TAKI DISPOSABLE ACUPUNCTURE NEEDLE receive FDA 510(k) clearance?
TAKI DISPOSABLE ACUPUNCTURE NEEDLE received FDA 510(k) clearance on 1996-07-26, under 510(k) number K962787.
Who is the listed applicant for TAKI DISPOSABLE ACUPUNCTURE NEEDLE?
The FDA 510(k) record lists Acupuncture Supplies Import Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAKI DISPOSABLE ACUPUNCTURE NEEDLE?
The FDA product code for TAKI DISPOSABLE 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.
Other records listing Acupuncture Supplies Import Co. 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.
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.
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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