TRIMPORT
K-Number: K974533 · 1998-05-07
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Device Summary
Frequently Asked Questions
What is the TRIMPORT?
TRIMPORT is a medical device that received FDA 510(k) clearance on 1998-05-07. The listed applicant is Gerard Medical, Inc.. The 510(k) number is K974533.
When did TRIMPORT receive FDA 510(k) clearance?
TRIMPORT received FDA 510(k) clearance on 1998-05-07, under 510(k) number K974533.
Who is the listed applicant for TRIMPORT?
The FDA 510(k) record lists Gerard Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRIMPORT?
The FDA product code for TRIMPORT is LJT.
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 Gerard Medical, 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: LJT)
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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