HANSO ACUPUNCTURE NEEDLE
K-Number: K090910 · 2009-06-30
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Device Summary
Frequently Asked Questions
What is the HANSO ACUPUNCTURE NEEDLE?
HANSO ACUPUNCTURE NEEDLE is a medical device that received FDA 510(k) clearance on 2009-06-30. The listed applicant is Hansol Medical Co.. The 510(k) number is K090910.
When did HANSO ACUPUNCTURE NEEDLE receive FDA 510(k) clearance?
HANSO ACUPUNCTURE NEEDLE received FDA 510(k) clearance on 2009-06-30, under 510(k) number K090910.
Who is the listed applicant for HANSO ACUPUNCTURE NEEDLE?
The FDA 510(k) record lists Hansol Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HANSO ACUPUNCTURE NEEDLE?
The FDA product code for HANSO 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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