BIOFEEDBACK SYSTEM/3
K-Number: K914920 · 1992-11-16
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Device Summary
Frequently Asked Questions
What is the BIOFEEDBACK SYSTEM/3?
BIOFEEDBACK SYSTEM/3 is a medical device that received FDA 510(k) clearance on 1992-11-16. The listed applicant is Davicon, Inc.. The 510(k) number is K914920.
When did BIOFEEDBACK SYSTEM/3 receive FDA 510(k) clearance?
BIOFEEDBACK SYSTEM/3 received FDA 510(k) clearance on 1992-11-16, under 510(k) number K914920.
Who is the listed applicant for BIOFEEDBACK SYSTEM/3?
The FDA 510(k) record lists Davicon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOFEEDBACK SYSTEM/3?
The FDA product code for BIOFEEDBACK SYSTEM/3 is HCC.
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 Davicon, 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: HCC)
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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