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FDA 510(k)

ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S

K-Number: K000740 · 2000-04-12

Decision Date2000-04-12
Product CodeMQX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S is the device name listed in this FDA 510(k) record. The listed applicant is Asahi Iryoki Co., Ltd.. It received FDA 510(k) clearance on 2000-04-12 under 510(k) number K000740. The device is classified under product code MQX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S?

ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S is a medical device that received FDA 510(k) clearance on 2000-04-12. The listed applicant is Asahi Iryoki Co., Ltd.. The 510(k) number is K000740.

When did ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S receive FDA 510(k) clearance?

ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S received FDA 510(k) clearance on 2000-04-12, under 510(k) number K000740.

Who is the listed applicant for ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S?

The FDA 510(k) record lists Asahi Iryoki Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S?

The FDA product code for ASAHI STERILE ACUPUNCTURE NEEDLE TYPE S 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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