YELLOW ALERT SYSTEM
K-Number: K791288 · 1979-08-03
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Device Summary
Frequently Asked Questions
What is the YELLOW ALERT SYSTEM?
YELLOW ALERT SYSTEM is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Hemoy, Inc.. The 510(k) number is K791288.
When did YELLOW ALERT SYSTEM receive FDA 510(k) clearance?
YELLOW ALERT SYSTEM received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791288.
Who is the listed applicant for YELLOW ALERT SYSTEM?
The FDA 510(k) record lists Hemoy, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for YELLOW ALERT SYSTEM?
The FDA product code for YELLOW ALERT SYSTEM is KGX.
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 Hemoy, 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: KGX)
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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