KHT SOFT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE
K-Number: K980470 · 1998-04-06
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Device Summary
Frequently Asked Questions
What is the KHT SOFT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE?
KHT SOFT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE is a medical device that received FDA 510(k) clearance on 1998-04-06. The listed applicant is American Institute of Koryo Hand Therapy. The 510(k) number is K980470.
When did KHT SOFT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE receive FDA 510(k) clearance?
KHT SOFT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE received FDA 510(k) clearance on 1998-04-06, under 510(k) number K980470.
Who is the listed applicant for KHT SOFT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE?
The FDA 510(k) record lists American Institute of Koryo Hand Therapy as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KHT SOFT SOOJI NEEDLE, HAND ACUPUNCTURE NEEDLE?
The FDA product code for KHT SOFT SOOJI NEEDLE, HAND 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.
Other records listing American Institute of Koryo Hand Therapy as applicant
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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