JIN ACUPUNCTURE NEEDLES, MODELS ST, GL, SI, PT, AND ID
K-Number: K980899 · 1998-06-11
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Device Summary
Frequently Asked Questions
What is the JIN ACUPUNCTURE NEEDLES, MODELS ST, GL, SI, PT, AND ID?
JIN ACUPUNCTURE NEEDLES, MODELS ST, GL, SI, PT, AND ID is a medical device that received FDA 510(k) clearance on 1998-06-11. The listed applicant is Kenshin Trading Corp.. The 510(k) number is K980899.
When did JIN ACUPUNCTURE NEEDLES, MODELS ST, GL, SI, PT, AND ID receive FDA 510(k) clearance?
JIN ACUPUNCTURE NEEDLES, MODELS ST, GL, SI, PT, AND ID received FDA 510(k) clearance on 1998-06-11, under 510(k) number K980899.
Who is the listed applicant for JIN ACUPUNCTURE NEEDLES, MODELS ST, GL, SI, PT, AND ID?
The FDA 510(k) record lists Kenshin Trading Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JIN ACUPUNCTURE NEEDLES, MODELS ST, GL, SI, PT, AND ID?
The FDA product code for JIN ACUPUNCTURE NEEDLES, MODELS ST, GL, SI, PT, AND ID 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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