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FDA 510(k)

EVT-3300

K-Number: K953621 · 1995-11-14

Decision Date1995-11-14
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EVT-3300 is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Table, Inc.. It received FDA 510(k) clearance on 1995-11-14 under 510(k) number K953621. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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