JIA CHEN ACUPUNCTURE NEEDLE, FOR SINGLE USE
K-Number: K023054 · 2002-11-13
Advertisement
Device Summary
Frequently Asked Questions
What is the JIA CHEN ACUPUNCTURE NEEDLE, FOR SINGLE USE?
JIA CHEN ACUPUNCTURE NEEDLE, FOR SINGLE USE is a medical device that received FDA 510(k) clearance on 2002-11-13. The listed applicant is Mandala Health Care, LLC. The 510(k) number is K023054.
When did JIA CHEN ACUPUNCTURE NEEDLE, FOR SINGLE USE receive FDA 510(k) clearance?
JIA CHEN ACUPUNCTURE NEEDLE, FOR SINGLE USE received FDA 510(k) clearance on 2002-11-13, under 510(k) number K023054.
Who is the listed applicant for JIA CHEN ACUPUNCTURE NEEDLE, FOR SINGLE USE?
The FDA 510(k) record lists Mandala Health Care, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JIA CHEN ACUPUNCTURE NEEDLE, FOR SINGLE USE?
The FDA product code for JIA CHEN ACUPUNCTURE NEEDLE, FOR SINGLE USE 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.
Advertisement