ACUSOURCE 600 FOR USE WITH TMJ ELECTRODE
K-Number: K901902 · 1990-10-09
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Device Summary
Frequently Asked Questions
What is the ACUSOURCE 600 FOR USE WITH TMJ ELECTRODE?
ACUSOURCE 600 FOR USE WITH TMJ ELECTRODE is a medical device that received FDA 510(k) clearance on 1990-10-09. The listed applicant is Microcurrent Research, Inc.. The 510(k) number is K901902.
When did ACUSOURCE 600 FOR USE WITH TMJ ELECTRODE receive FDA 510(k) clearance?
ACUSOURCE 600 FOR USE WITH TMJ ELECTRODE received FDA 510(k) clearance on 1990-10-09, under 510(k) number K901902.
Who is the listed applicant for ACUSOURCE 600 FOR USE WITH TMJ ELECTRODE?
The FDA 510(k) record lists Microcurrent Research, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACUSOURCE 600 FOR USE WITH TMJ ELECTRODE?
The FDA product code for ACUSOURCE 600 FOR USE WITH TMJ ELECTRODE is NUW.
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 Microcurrent Research, 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: NUW)
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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