T-CONNECTOR
K-Number: K790408 · 1979-04-30
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Device Summary
Frequently Asked Questions
What is the T-CONNECTOR?
T-CONNECTOR is a medical device that received FDA 510(k) clearance on 1979-04-30. The listed applicant is Medex, Inc.. The 510(k) number is K790408.
When did T-CONNECTOR receive FDA 510(k) clearance?
T-CONNECTOR received FDA 510(k) clearance on 1979-04-30, under 510(k) number K790408.
Who is the listed applicant for T-CONNECTOR?
The FDA 510(k) record lists Medex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for T-CONNECTOR?
The FDA product code for T-CONNECTOR is FPA.
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 Medex, 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: FPA)
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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