SHENLING ACUPUNCTURE NEEDLES
K-Number: K002411 · 2000-12-12
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Device Summary
Frequently Asked Questions
What is the SHENLING ACUPUNCTURE NEEDLES?
SHENLING ACUPUNCTURE NEEDLES is a medical device that received FDA 510(k) clearance on 2000-12-12. The listed applicant is Shenling Medical Device Co., Ltd.. The 510(k) number is K002411.
When did SHENLING ACUPUNCTURE NEEDLES receive FDA 510(k) clearance?
SHENLING ACUPUNCTURE NEEDLES received FDA 510(k) clearance on 2000-12-12, under 510(k) number K002411.
Who is the listed applicant for SHENLING ACUPUNCTURE NEEDLES?
The FDA 510(k) record lists Shenling Medical Device Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHENLING ACUPUNCTURE NEEDLES?
The FDA product code for SHENLING 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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