MEDCOMP T-3
K-Number: K033570 · 2004-09-16
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Device Summary
Frequently Asked Questions
What is the MEDCOMP T-3?
MEDCOMP T-3 is a medical device that received FDA 510(k) clearance on 2004-09-16. The listed applicant is Medcomp. The 510(k) number is K033570.
When did MEDCOMP T-3 receive FDA 510(k) clearance?
MEDCOMP T-3 received FDA 510(k) clearance on 2004-09-16, under 510(k) number K033570.
Who is the listed applicant for MEDCOMP T-3?
The FDA 510(k) record lists Medcomp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDCOMP T-3?
The FDA product code for MEDCOMP T-3 is NIE.
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 Medcomp 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: NIE)
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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