HWA-TO ACUPUNCTURE NEEDLES
K-Number: K963299 · 1996-09-30
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Device Summary
Frequently Asked Questions
What is the HWA-TO ACUPUNCTURE NEEDLES?
HWA-TO ACUPUNCTURE NEEDLES is a medical device that received FDA 510(k) clearance on 1996-09-30. The listed applicant is Lhasa Medical, Inc.. The 510(k) number is K963299.
When did HWA-TO ACUPUNCTURE NEEDLES receive FDA 510(k) clearance?
HWA-TO ACUPUNCTURE NEEDLES received FDA 510(k) clearance on 1996-09-30, under 510(k) number K963299.
Who is the listed applicant for HWA-TO ACUPUNCTURE NEEDLES?
The FDA 510(k) record lists Lhasa Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HWA-TO ACUPUNCTURE NEEDLES?
The FDA product code for HWA-TO 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.
Other records listing Lhasa Medical, Inc. 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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