VINCO BRAND ACUPUNCTURE NEEDLE
K-Number: K024207 · 2003-04-14
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Device Summary
Frequently Asked Questions
What is the VINCO BRAND ACUPUNCTURE NEEDLE?
VINCO BRAND ACUPUNCTURE NEEDLE is a medical device that received FDA 510(k) clearance on 2003-04-14. The listed applicant is Helio Medical Supplies, Inc.. The 510(k) number is K024207.
When did VINCO BRAND ACUPUNCTURE NEEDLE receive FDA 510(k) clearance?
VINCO BRAND ACUPUNCTURE NEEDLE received FDA 510(k) clearance on 2003-04-14, under 510(k) number K024207.
Who is the listed applicant for VINCO BRAND ACUPUNCTURE NEEDLE?
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 VINCO BRAND ACUPUNCTURE NEEDLE?
The FDA product code for VINCO BRAND 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 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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