HEMATRAK MODEL 480
K-Number: K790816 · 1979-07-17
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Device Summary
Frequently Asked Questions
What is the HEMATRAK MODEL 480?
HEMATRAK MODEL 480 is a medical device that received FDA 510(k) clearance on 1979-07-17. The listed applicant is Geometric Data, Div. Smithkline Corp.. The 510(k) number is K790816.
When did HEMATRAK MODEL 480 receive FDA 510(k) clearance?
HEMATRAK MODEL 480 received FDA 510(k) clearance on 1979-07-17, under 510(k) number K790816.
Who is the listed applicant for HEMATRAK MODEL 480?
The FDA 510(k) record lists Geometric Data, Div. Smithkline Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMATRAK MODEL 480?
The FDA product code for HEMATRAK MODEL 480 is GKZ.
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 Geometric Data, Div. Smithkline Corp. 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: GKZ)
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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