EVA EMPTY SOLUTION CONTAINER
K-Number: K030888 · 2003-04-02
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Device Summary
Frequently Asked Questions
What is the EVA EMPTY SOLUTION CONTAINER?
EVA EMPTY SOLUTION CONTAINER is a medical device that received FDA 510(k) clearance on 2003-04-02. The listed applicant is Metrix Co.. The 510(k) number is K030888.
When did EVA EMPTY SOLUTION CONTAINER receive FDA 510(k) clearance?
EVA EMPTY SOLUTION CONTAINER received FDA 510(k) clearance on 2003-04-02, under 510(k) number K030888.
Who is the listed applicant for EVA EMPTY SOLUTION CONTAINER?
The FDA 510(k) record lists Metrix Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EVA EMPTY SOLUTION CONTAINER?
The FDA product code for EVA EMPTY SOLUTION CONTAINER is KPE.
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 Metrix Co. 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: KPE)
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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