H.M.T. ACUPUNCTURE NEEDLE
K-Number: K012501 · 2001-12-11
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Device Summary
Frequently Asked Questions
What is the H.M.T. ACUPUNCTURE NEEDLE?
H.M.T. ACUPUNCTURE NEEDLE is a medical device that received FDA 510(k) clearance on 2001-12-11. The listed applicant is Hummingbird Medical Technology, LLC. The 510(k) number is K012501.
When did H.M.T. ACUPUNCTURE NEEDLE receive FDA 510(k) clearance?
H.M.T. ACUPUNCTURE NEEDLE received FDA 510(k) clearance on 2001-12-11, under 510(k) number K012501.
Who is the listed applicant for H.M.T. ACUPUNCTURE NEEDLE?
The FDA 510(k) record lists Hummingbird Medical Technology, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for H.M.T. ACUPUNCTURE NEEDLE?
The FDA product code for H.M.T. 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.
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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