EVT-3300
K-Number: K953621 · 1995-11-14
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Device Summary
Frequently Asked Questions
What is the EVT-3300?
EVT-3300 is a medical device that received FDA 510(k) clearance on 1995-11-14. The listed applicant is U.S. Table, Inc.. The 510(k) number is K953621.
When did EVT-3300 receive FDA 510(k) clearance?
EVT-3300 received FDA 510(k) clearance on 1995-11-14, under 510(k) number K953621.
Who is the listed applicant for EVT-3300?
The FDA 510(k) record lists U.S. Table, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EVT-3300?
The FDA product code for EVT-3300 is INQ.
Other records listing U.S. Table, 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: INQ)
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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