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FDA 510(k)

TRIMPORT

K-Number: K974533 · 1998-05-07

Decision Date1998-05-07
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRIMPORT is the device name listed in this FDA 510(k) record. The listed applicant is Gerard Medical, Inc.. It received FDA 510(k) clearance on 1998-05-07 under 510(k) number K974533. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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