ANALOG QUANTIFIER MODEL AQ-100
K-Number: K771023 · 1977-06-24
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Device Summary
Frequently Asked Questions
What is the ANALOG QUANTIFIER MODEL AQ-100?
ANALOG QUANTIFIER MODEL AQ-100 is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is Bio-Feedback Systems, Inc.. The 510(k) number is K771023.
When did ANALOG QUANTIFIER MODEL AQ-100 receive FDA 510(k) clearance?
ANALOG QUANTIFIER MODEL AQ-100 received FDA 510(k) clearance on 1977-06-24, under 510(k) number K771023.
Who is the listed applicant for ANALOG QUANTIFIER MODEL AQ-100?
The FDA 510(k) record lists Bio-Feedback Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANALOG QUANTIFIER MODEL AQ-100?
The FDA product code for ANALOG QUANTIFIER MODEL AQ-100 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 Bio-Feedback Systems, 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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