PERCEPTOR
K-Number: K770321 · 1977-02-28
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Device Summary
Frequently Asked Questions
What is the PERCEPTOR?
PERCEPTOR is a medical device that received FDA 510(k) clearance on 1977-02-28. The listed applicant is Danavox, Inc.. The 510(k) number is K770321.
When did PERCEPTOR receive FDA 510(k) clearance?
PERCEPTOR received FDA 510(k) clearance on 1977-02-28, under 510(k) number K770321.
Who is the listed applicant for PERCEPTOR?
The FDA 510(k) record lists Danavox, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERCEPTOR?
The FDA product code for PERCEPTOR is ESD.
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 Danavox, 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: ESD)
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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