ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLES
K-Number: K981272 · 1998-08-24
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Device Summary
Frequently Asked Questions
What is the ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLES?
ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLES is a medical device that received FDA 510(k) clearance on 1998-08-24. The listed applicant is Electro Therapeutic Devices, Inc.. The 510(k) number is K981272.
When did ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLES receive FDA 510(k) clearance?
ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLES received FDA 510(k) clearance on 1998-08-24, under 510(k) number K981272.
Who is the listed applicant for ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLES?
The FDA 510(k) record lists Electro Therapeutic Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLES?
The FDA product code for ADDIQUIP DISPOSABLE 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 Electro Therapeutic Devices, 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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