HOLY DRAGON BRAND ACUPUNCTURE NEEDLES
K-Number: K021095 · 2002-05-17
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Device Summary
Frequently Asked Questions
What is the HOLY DRAGON BRAND ACUPUNCTURE NEEDLES?
HOLY DRAGON BRAND ACUPUNCTURE NEEDLES is a medical device that received FDA 510(k) clearance on 2002-05-17. The listed applicant is Wujiang City Hua Xin Medical Appliance Co., Ltd.. The 510(k) number is K021095.
When did HOLY DRAGON BRAND ACUPUNCTURE NEEDLES receive FDA 510(k) clearance?
HOLY DRAGON BRAND ACUPUNCTURE NEEDLES received FDA 510(k) clearance on 2002-05-17, under 510(k) number K021095.
Who is the listed applicant for HOLY DRAGON BRAND ACUPUNCTURE NEEDLES?
The FDA 510(k) record lists Wujiang City Hua Xin Medical Appliance Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HOLY DRAGON BRAND ACUPUNCTURE NEEDLES?
The FDA product code for HOLY DRAGON BRAND 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.
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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