BRIO ACUPUNCTURE NEEDLES
K-Number: K072778 · 2007-11-19
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Device Summary
Frequently Asked Questions
What is the BRIO ACUPUNCTURE NEEDLES?
BRIO ACUPUNCTURE NEEDLES is a medical device that received FDA 510(k) clearance on 2007-11-19. The listed applicant is Helio Medical Supplies, Inc.. The 510(k) number is K072778.
When did BRIO ACUPUNCTURE NEEDLES receive FDA 510(k) clearance?
BRIO ACUPUNCTURE NEEDLES received FDA 510(k) clearance on 2007-11-19, under 510(k) number K072778.
Who is the listed applicant for BRIO ACUPUNCTURE NEEDLES?
The FDA 510(k) record lists Helio Medical Supplies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRIO ACUPUNCTURE NEEDLES?
The FDA product code for BRIO 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 Helio Medical Supplies, 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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