ACUBAND ACUPRESSURE WRIST BAND DEVICE
K-Number: K053509 · 2006-08-16
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Device Summary
Frequently Asked Questions
What is the ACUBAND ACUPRESSURE WRIST BAND DEVICE?
ACUBAND ACUPRESSURE WRIST BAND DEVICE is a medical device that received FDA 510(k) clearance on 2006-08-16. The listed applicant is Acuband, Inc.. The 510(k) number is K053509.
When did ACUBAND ACUPRESSURE WRIST BAND DEVICE receive FDA 510(k) clearance?
ACUBAND ACUPRESSURE WRIST BAND DEVICE received FDA 510(k) clearance on 2006-08-16, under 510(k) number K053509.
Who is the listed applicant for ACUBAND ACUPRESSURE WRIST BAND DEVICE?
The FDA 510(k) record lists Acuband, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACUBAND ACUPRESSURE WRIST BAND DEVICE?
The FDA product code for ACUBAND ACUPRESSURE WRIST BAND DEVICE is MVV.
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: MVV)
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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