MODEL 379 FLOW/DIVIDER
K-Number: K821520 · 1982-06-02
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Device Summary
Frequently Asked Questions
What is the MODEL 379 FLOW/DIVIDER?
MODEL 379 FLOW/DIVIDER is a medical device that received FDA 510(k) clearance on 1982-06-02. The listed applicant is Marathon. The 510(k) number is K821520.
When did MODEL 379 FLOW/DIVIDER receive FDA 510(k) clearance?
MODEL 379 FLOW/DIVIDER received FDA 510(k) clearance on 1982-06-02, under 510(k) number K821520.
Who is the listed applicant for MODEL 379 FLOW/DIVIDER?
The FDA 510(k) record lists Marathon as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 379 FLOW/DIVIDER?
The FDA product code for MODEL 379 FLOW/DIVIDER is CAW.
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 Marathon 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: CAW)
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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