ECHO CARDIOGRAM PAD
K-Number: K791189 · 1979-07-17
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Device Summary
Frequently Asked Questions
What is the ECHO CARDIOGRAM PAD?
ECHO CARDIOGRAM PAD is a medical device that received FDA 510(k) clearance on 1979-07-17. The listed applicant is Alimed, Inc.. The 510(k) number is K791189.
When did ECHO CARDIOGRAM PAD receive FDA 510(k) clearance?
ECHO CARDIOGRAM PAD received FDA 510(k) clearance on 1979-07-17, under 510(k) number K791189.
Who is the listed applicant for ECHO CARDIOGRAM PAD?
The FDA 510(k) record lists Alimed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ECHO CARDIOGRAM PAD?
The FDA product code for ECHO CARDIOGRAM PAD is FNJ.
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 Alimed, 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: FNJ)
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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