BW ACUPUNCTURE NEEDLES
K-Number: K011669 · 2001-07-09
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Device Summary
Frequently Asked Questions
What is the BW ACUPUNCTURE NEEDLES?
BW ACUPUNCTURE NEEDLES is a medical device that received FDA 510(k) clearance on 2001-07-09. The listed applicant is H F Intl. Co.. The 510(k) number is K011669.
When did BW ACUPUNCTURE NEEDLES receive FDA 510(k) clearance?
BW ACUPUNCTURE NEEDLES received FDA 510(k) clearance on 2001-07-09, under 510(k) number K011669.
Who is the listed applicant for BW ACUPUNCTURE NEEDLES?
The FDA 510(k) record lists H F Intl. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BW ACUPUNCTURE NEEDLES?
The FDA product code for BW 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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